Medicininės klasės tamprus sidabro spalvos poliesterio tinklelio tvarstis
- Innovative Polymer Silver Complex (>0.25mg/g) for Long-Lasting Antibacterial Protection
- Soft Skin-Friendly Polyester Mesh with Elastic Stretch for Contour Fit
- High Breathability & Efficient Exudate Wicking for Moist Wound Healing
- Anti-Adhesion Formula (White Petrolatum & Paraffin Oil) for Painless Removal
- Cuttable Design for Custom Wound Sizing (Extend 2cm Beyond Wound Edges)
- NPWT Compatible - Ideal as a Contact Layer for Negative Pressure Wound Therapy
- ISO 13485:2016 Certified & Irradiation Sterilized (Sterile Single-Use)
- Visuotinis pritaikymas ir reguliavimo techniniai dokumentai vietinei registracijai
Prekės Įvadas
This Silver Polyester Mesh Dressing is an advanced antimicrobial wound care solution that combines high-performance polymer silver complex technology with a soft, stretchable medical-grade polyester mesh structure—engineered for the effective management of acute and chronic wounds, and specially optimized for compatibility with negative pressure wound therapy (NPWT). Designed for clinical use in hospitals, wound care centers and post-operative care, it is the perfect choice for 1st & 2nd degree burns, graft/donor site coverage, surgical wounds, pressure ulcers (PUs), venous leg ulcers (VLUs), diabetic foot ulcers (DFUs) and traumatic wounds with moderate to heavy exudate.
Crafted with a special elastic knitting process, the skin-friendly polyester mesh conforms perfectly to uneven and irregular wound contours, ensuring full contact and coverage without causing skin irritation or discomfort—even on mobile body parts (e.g., joints, limbs). Infused with a polymer silver complex (>0.25mg/g), the dressing delivers broad-spectrum, long-lasting antimicrobial protection, forming a physical and antibacterial barrier on the wound surface to inhibit Staphylococcus aureus, Escherichia coli, Candida albicans and other common wound pathogens, while eliminating the risk of antibiotic resistance.
The breathable mesh structure enables efficient exudate wicking and moisture evaporation, maintaining an optimal moist wound healing environment and preventing fluid buildup that can lead to bacterial colonization. Infused with white petrolatum and paraffin oil, it features superior anti-adhesion properties, allowing for painless dressing changes and reducing secondary damage to fragile granulation tissue. Sterilized by irradiation, single-use, and easily cut to custom sizes, this dressing is also the gold standard contact layer for NPWT, providing a soft antibacterial interface between the wound bed and NPWT devices. For global distributors and clinical partners, we offer fully customizable packaging and a complete set of regulatory-compliant technical documents, supporting seamless local product registration and market access across the EU, Middle East, Asia, Africa and all global regions.
Techninės specifikacijos
| Punktas | detalizavimas |
| Prekės kodas | ACTC01 / ACTC02 / ACTC03 / ACTC04 / ACTC05 |
| Dydžiai | 5cm×5cm, 10cm×10cm, 10cm×20cm, 20cm×40cm, 40cm×40cm |
| Pagrindinė medžiaga | Medical-grade stretchable polyester mesh, polymer silver complex (>0.25mg/g), white petrolatum, paraffin oil |
| Pagrindinės technologijos | Polymer silver complex antimicrobial, elastic special knitting process, high-efficiency exudate wicking |
| Antibakterinis spektras | Plataus spektro (Staphylococcus aureus, Escherichia coli, Candida albicans) |
| Aprangos ypatybės | Stretchable/contour fit, breathable, anti-adhesion, cuttable, NPWT compatible, sterile single-use |
| Tinkamos žaizdos | 1st/2nd degree burns, graft/donor sites, surgical wounds, pressure ulcers, venous leg ulcers, diabetic foot ulcers, traumatic wounds, NPWT contact layer for all wound types |
| Sterilizavimo metodas | Sterilizacija spinduliais (garantuota 100 % sterilumas) |
| Pakuotės tipas | Individuali sterili sandari pakuotė (medicininės klasės apsauginė plėvelė) |
| Kartoninė pakuotė | 10 vnt./dėžutėje, klinikinė/ligoninės pakuotė dideliems kiekiams |
| Tinkinamos parinktys | Custom sizes, multilingual packaging printing, branded sterile labels |
| Tinkamumo laikas | 3 metai nuo pagaminimo datos (tiksli galiojimo data nurodyta ant pakuotės) |
| Laikymo sąlygos | Store in a dry, cool place; protect from direct light, high temperature and high humidity |
| Sertifikuotas | Sertifikuota medicinos prietaisų kokybės vadybos sistema pagal ISO 13485:2016 |
| Reguliavimo laikymasis | Palaiko techninių dokumentų pritaikymą pasaulinei medicinos prietaisų registracijai (ES, Artimieji Rytai, Pietryčių Azija, Afrika ir kt.) |
Kaip naudotis
- For Standard Clinical Wound Care (Hospitals/Clinics)
- 1. Follow strict aseptic technique for all application and handling steps.
- 2. Disinfect the skin surrounding the wound with a medical antiseptic, rinse thoroughly with sterile normal saline to remove debris, exudate or necrotic tissue, and pat the area completely dry.
- 3. Open the sterile packaging and remove the silver polyester mesh dressing—no backing to peel (ready for direct application).
- 4. Cut the dressing to custom size with sterile scissors, ensuring it extends at least 2cm beyond all edges of the wound for full antimicrobial protection.
- 5. Gently apply the dressing directly over the entire wound surface, pressing lightly to ensure optimal contact (no stretching required).
- 6. Secure the dressing with a suitable secondary dressing (e.g., gauze, non-woven bandage) or compression therapy; adjust fixation based on wound location and exudate volume.
- 7. Change the dressing according to wound exudate amount and clinical condition (2-3 days for moderate exudate; daily for heavy exudate) or as directed by a physician.
- For Use as a NPWT Contact Layer (Under Professional Guidance)
- 1. Prepare the wound as directed (aseptic cleaning, disinfection and drying) and follow NPWT device manufacturer’s pre-application guidelines.
- 2. Cut the silver polyester mesh dressing to fit the wound (extend 2cm beyond wound edges) and apply it as the primary contact layer directly over the wound bed.
- 3. Position the NPWT foam/drape over the dressing as instructed, ensuring proper sealing of the NPWT device.
- 4. Initiate NPWT therapy per clinical protocol; monitor the wound and dressing daily for exudate buildup or device leakage.
- 5. Change the dressing and NPWT foam as recommended by the physician or NPWT device guidelines (typically every 2-5 days).
Visuotinis pritaikymas ir atitikties palaikymas
- 1. Pritaikomos produktų ir pakuočių parinktys
- Dressing Customization: Custom cut sizes for specialized clinical use (e.g., large size for extensive burns, small size for facial wounds)
- Sterilios pakuotės pritaikymas: medicininės klasės sterili apsauginė plėvelė su daugiakalbe spauda (produkto instrukcijos, prekės ženklo logotipas, vietiniai reglamentų ženklai); individualiai pritaikytos sterilios etiketės klinikiniam / ligoninės prekės ženklui.
- Bulk Carton Customization: Branded carton design, batch number/lot code printing, clinical packaging specification adjustment, enhanced transportation protection for long-distance/global shipping
- MOQ lankstumas: mažas minimalus užsakymo kiekis mažiems / vidutiniams platintojams; lengvatinės didmeninės kainos ir išskirtinis pritaikymas didelėms ligoninėms / medicinos įstaigoms
- 2. Reglamentus atitinkantys techniniai dokumentai
- ISO 13485:2016 kokybės vadybos sistemos sertifikavimo dokumentas
- Product Technical Specification (TS) with full antibacterial, biocompatibility and performance test data (polymer silver complex efficacy, exudate wicking, stretchability)
- Klinikinio patvirtinimo ataskaita ir in vitro antibakterinio veiksmingumo tyrimo ataskaita
- Švitinimo sterilizavimo sertifikavimas ir partijos kokybės patikros sertifikatas
- Medžiagos saugos duomenų lapas (MSDS)
- Multilingual Product Instructions (clinical/professional version) & Labeling Compliance Document
- NPWT Compatibility Verification Report (for clinical/registration use)
Siūlome lanksčias, klinikinės klasės pritaikymo paslaugas, pritaikytas unikaliems pasaulinių platintojų, ligoninių, žaizdų priežiūros centrų ir medicinos įstaigų poreikiams – su mažu minimalų užsakymo kiekiu ir be nereikalingų liejimo formų išlaidų standartiniams pritaikymams:
Mūsų profesionali reguliavimo komanda teikia visą standartizuotų techninių dokumentų rinkinį, atitinkantį ISO 13485:2016 ir regioninius medicinos prietaisų reglamentus (ES, Artimųjų Rytų, Pietryčių Azijos, Afrikos, Šiaurės Amerikos ir kt.). Visus dokumentus galima visiškai pritaikyti ir papildyti, kad jie atitiktų vietinius registracijos reikalavimus, o nemokami atnaujinimai atitinka atnaujintus reguliavimo standartus, įskaitant, bet neapsiribojant:
Pritaikymas ir dokumentų aptarnavimas pagal kliento tipą
| Kliento tipas | Mažiausias užsakymo kiekis (MOQ) | Individualaus aprengimo / pakavimo palaikymas | Techninių dokumentų tarnyba |
| Maži / vidutiniai platintojai | ≥50 dėžių (viena specifikacija) | Individuali pakuotės spauda + dydžio pasirinkimas (be liejimo išlaidų) | Nemokami pagrindiniai pasaulinės atitikties dokumentai + vertimas į kelias kalbas |
| Regioniniai klinikiniai platintojai | ≥200 dėžių (viena specifikacija) | Visiškas pritaikymas (nestandartiniai dydžiai + sterili pakuotė + kartono dizainas) | Nemokami lokalizuoti norminiai dokumentai + produkto registracijos gairės |
| Didelės ligoninės / medicinos įstaigos | ≥500 dėžių (viena specifikacija) | Išskirtinis OEM/ODM + specializuotas klinikinių variantų pritaikymas | Nemokami išskirtiniai norminiai dokumentai + specialus registracijos konsultantas + metiniai dokumentų atnaujinimai |
Atsargumo priemonės
1. Tik išoriniam klinikiniam naudojimui; nenaudokite ant neužgijusių gilių žaizdų, sunkiai nekrozinių žaizdų arba žaizdų, kurioms nekontroliuojamas gausus kraujavimas, be gydytojo ar žaizdų priežiūros specialisto nurodymų.
2. Viso tvarsčio uždėjimo, pjovimo ir tvarkymo metu laikykitės aseptikos taisyklių, kad išvengtumėte antrinės žaizdos infekcijos; pakartotinai nenaudokite sterilaus vienkartinio tvarsčio.
3. Discontinue use immediately and consult a physician if the wound shows signs of worsening (e.g., increased redness, swelling, pain, exudate, odor or fever) after application.
4. Keep out of reach of non-clinical personnel/children; store the dressing in the original sterile packaging until use to maintain sterility and silver ion activity.
5. Do not use the product if the sterile packaging is damaged, torn, punctured or the seal is broken—sterility cannot be guaranteed.
6. Venkite patekimo į akis ir burnos / nosies gleivinę; atsitiktinai patekus į akis, nedelsiant kruopščiai praplaukite dideliu kiekiu sterilaus fiziologinio tirpalo ir, jei dirginimas nepraeina, kreipkitės į sveikatos priežiūros specialistą.
7. This product is not suitable for individuals with a known allergy to silver ions, polyester, white petrolatum, paraffin oil or any other ingredients in the dressing.
8. Nenaudokite kartu su kitais vietinio poveikio antimikrobiniais žaizdų priežiūros produktais be gydytojo ar klinikinio žaizdų priežiūros specialisto nurodymų.
9. Follow the specified storage conditions; do not store in high temperature (>30℃), high humidity (>70%RH) or direct sunlight—may affect polymer silver complex activity and dressing performance.
10. When using as a NPWT contact layer, strictly follow the NPWT device manufacturer’s guidelines and clinical physician instructions; do not modify the dressing or NPWT setup without professional guidance.
Kontaktai
- Klinikinis verslo bendradarbiavimas ir konsultacijos dėl didmeninių pirkimų
- "WhatsApp": https://wa.me/8617788969619 | https://wa.me/8619173969821
- Mobilusis / „WeChat“: +86-19173969821 | +86-17788969619
- Oficialus klinikinis el. pašto adresas: [apsaugotas el. paštu] | [apsaugotas el. paštu]
- Adresas: 5-8 aukštas, A4 tarptautinis medicinos instrumentų pramonės parkas, Nr. 229 Hunano Lugu kelias, Čangšos aukštųjų technologijų plėtros zona, Čangša, Hunanas, Kinija
- Visuotinis pritaikymas ir konsultacijos dėl norminių dokumentų (speciali klinikinė linija)
- Atsakingas konsultantas (WeChat/WhatsApp): +86-19173969821
- Service Scope: Dressing customization, packaging design, local product registration document preparation, NPWT compatibility verification, regulatory compliance guidance
DUK
Q1: What makes this silver polyester mesh dressing different from silver cotton mesh dressing?
A1: This polyester mesh dressing features stretchable/elastic properties for a perfect fit on irregular/contoured wound sites (e.g., joints, limbs) and higher breathability for efficient exudate wicking—ideal for moderate-heavy exudate wounds and NPWT use. Silver cotton mesh dressing is non-stretch and better suited for low-moderate exudate wounds on flat body parts. Both deliver broad-spectrum antibacterial protection, but the polyester variant is optimized for mobility and NPWT compatibility.
Q2: Can this dressing be used on all wound types for NPWT, or only specific ones?
A2: It is suitable as a NPWT contact layer for most acute and chronic wounds (surgical wounds, burns, pressure ulcers, venous ulcers, traumatic wounds) with mild to heavy exudate. It is not recommended for wounds with severe necrosis or uncontrolled bleeding—these require prior debridement and professional physician assessment before NPWT and dressing application.
Q3: How does the polymer silver complex (>0.25mg/g) ensure long-lasting antibacterial protection?
A3: The polymer silver complex is uniformly infused into the polyester mesh structure, creating a slow-release antimicrobial system that delivers active silver ions to the wound surface for up to 72 hours per application. This sustained release ensures continuous antibacterial protection, unlike fast-release silver dressings that lose efficacy quickly, and avoids irritation to new granulation tissue from sudden silver ion release.
Q4: Is the stretchable polyester mesh comfortable for long-term wear on mobile body parts (e.g., knees, elbows)?
A4: Yes. The special elastic knitting process makes the mesh soft, flexible and highly stretchable, conforming to the natural movement of joints and limbs without causing skin irritation, tightness or dressing displacement. It maintains full contact with the wound surface during movement, ensuring uninterrupted antimicrobial protection and exudate wicking.
Q5: What is the recommended dressing change frequency for different wound exudate levels?
A5: For mild exudate wounds (e.g., small surgical incisions, shallow burns): change every 2-3 days; for moderate exudate wounds (e.g., early-stage ulcers, graft sites): change daily; for heavy exudate wounds (e.g., advanced venous ulcers, large burns): change 1-2 times daily or as directed by a physician. Always adjust based on clinical wound condition and exudate buildup.
Q6: Does this dressing require refrigeration for storage or international transportation (e.g., to high-temperature regions like the Middle East)?
A6: No. This dressing is a room temperature-stable medical device—refrigeration is not required and may cause condensation that damages sterile packaging. For international transportation to high-temperature regions, we recommend insulated shipping cartons to avoid prolonged exposure to extreme heat (>40℃), which aligns with our storage condition guidelines (dry, cool, protected from light).
Q7: Can the dressing be cut to any size, and does cutting affect its antibacterial performance?
A7: Yes, it can be cut to any custom size with sterile scissors (aseptic technique required) to fit all wound shapes and sizes. Cutting does not affect the antibacterial performance— the polymer silver complex is uniformly infused throughout the entire mesh structure, so all cut edges and surfaces retain full antimicrobial protection.
Q8: Do you provide clinical training for staff on using this dressing as a NPWT contact layer?
A8: Yes. For bulk clinical procurement by hospitals/wound care centers, we provide free online clinical application training (conducted by our wound care and NPWT specialists) covering aseptic application, custom cutting, NPWT setup compatibility and troubleshooting. We also provide a printable multilingual clinical application guide for on-site staff training and reference.
9 klausimas: Koks yra standartinių birių užsakymų ir nestandartinių dydžių / pakuočių užsakymų pristatymo laikas?
A9: For standard non-customized bulk orders (all original sizes), the lead time is 15 working days. For custom size/packaging orders (custom cutting, multilingual printing, branded packaging), the lead time is 60 working days (no mold cost for standard customizations). For large hospital/institutional bulk orders (≥500 cartons), we offer flexible lead time adjustments and priority production scheduling.
Q10: Is this dressing suitable for pediatric and geriatric patients with sensitive skin?
A10: Yes. The soft skin-friendly polyester mesh is hypoallergenic and non-irritating, making it safe for use on pediatric and geriatric patients with sensitive or fragile skin. The anti-adhesion formula also ensures painless dressing changes, which is critical for pediatric patients and geriatric patients with reduced skin elasticity. As with all medical devices, use under adult/physician supervision for pediatric patients.






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