Changsha Hairun Biotechnology Co., Ltd.
Sidabro jonų medvilninio tinklelio tvarstis

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Medicininės klasės HBP sidabro jonų medvilninio tinklelio tvarstis – ilgalaikio atpalaidavimo antibakterinis tvarstis infekuotoms žaizdoms ir opoms


Advanced HBP Silver Ion Chelation Technology (Controlled Sustained Release)
100% Soft Medical Cotton Mesh with Double Knitting for Optimal Drainage
Anti-Adhesion Formula (White Petrolatum & Paraffin Oil) for Painless Dressing Change
Broad-Spectrum Antibacterial (Targets S. aureus, E. coli, C. albicans)
Sterile Single-Use Packaging to Prevent Cross-Contamination
Cuttable Design for Custom Fit to All Wound Contours
ISO 13485:2016 Certified & Compliant with Global Medical Device Standards
One-Stop Customization & Technical Documents for Local Registration
Prekės Įvadas

This Silver Ion Cotton Mesh Dressing is a high-performance antimicrobial wound care solution engineered with innovative Hyperbranched Polymers (HBP) Ag+ chelation technology—the gold standard for treating infected acute and chronic wounds. Specially designed for clinical use in hospitals, clinics and wound care centers, it is the ideal choice for managing venous leg ulcers (VLUs), pressure ulcers (PUs), diabetic foot ulcers (DFUs), 1st & 2nd degree burns, surgical wounds, traumatic abrasions and donor site care.

Crafted from soft, medical-grade cotton with a double warp and weft knitting process, the dressing features large mesh cells that enable efficient exudate drainage, preventing fluid buildup and bacterial overgrowth in the wound bed. The HBP Ag+ core technology chelates silver ions via functional groups and releases them in a controlled, sustained manner through ion exchange—ensuring long-lasting antibacterial activity without sudden release irritation to new granulation tissue. This non-antibiotic formulation forms a durable antimicrobial barrier on the wound surface, inhibiting a broad spectrum of common wound pathogens (including Staphylococcus aureus, Escherichia coli and Candida albicans) and eliminating the risk of bacterial resistance.

Infused with white petrolatum and paraffin oil, the dressing delivers superior anti-adhesion performance, allowing for painless removal and reducing secondary damage to fragile wound tissue. Sterile, single-use and easy to apply, it conforms perfectly to irregular wound contours and can be used as both a primary and secondary dressing for infected wounds of all sizes. For global distributors and clinical partners, we provide 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 beyond.

Techninės specifikacijos
Punktas detalizavimas
Prekės kodas SAFD15 / SAFD16 / SAFD17 / SAFD18
Dydžiai 5cm×5cm, 10cm×10cm, 15cm×15cm, 20cm×20cm
Pagrindinė medžiaga Medical-grade cotton mesh, Hyperbranched Polymers (HBP) Ag+ complex, white petrolatum, paraffin oil
Pagrindinės technologijos HBP silver ion chelation, ion exchange controlled sustained release
Antibakterinis spektras Staphylococcus aureus, Escherichia coli, Candida albicans (broad-spectrum)
Aprangos ypatybės Double knitting, large mesh drainage, anti-adhesion, sterile, single-use, cuttable
Tinkamos žaizdos Infected acute/chronic wounds, venous leg ulcers (VLUs), pressure ulcers (PUs), diabetic foot ulcers (DFUs), 1st/2nd degree burns, surgical wounds, traumatic abrasions, donor sites
Sterilizavimo metodas Irradiation sterilization (sterile guaranteed)
Pakuotės tipas Individual sterile sealed packaging
Kartoninė pakuotė 10 pieces/box, standard clinical bulk pack
Tinkinamos parinktys Oily/non-oily variants, custom sizes, packaging printing/design
Tinkamumo laikas 3 years from production date (see packaging for exact expiration)
Laikymo sąlygos Store in a dry, cool place; protect from direct light and high temperature; avoid humidity
Sertifikuotas Sertifikuota medicinos prietaisų kokybės vadybos sistema pagal ISO 13485:2016
Reguliavimo laikymasis Supports technical document customization for global medical device registration
Kaip naudotis
For Clinical Professional Use (Hospitals/Clinics)
Adhere to strict aseptic technique throughout all application steps.
Disinfect the skin surrounding the wound with a medical-grade antiseptic, rinse thoroughly with sterile normal saline to remove debris and exudate, and pat the area completely dry.
Open the sterile packaging and remove the silver ion cotton mesh dressing; peel off the backing to expose the adhesive surface (for adhesive variants).
Place the dressing over the wound, ensuring full coverage of the wound bed and a 1-2cm extension onto healthy surrounding skin.
Press the dressing firmly onto the skin, starting from the center of the wound and working outward to the edges, to ensure optimal adhesion and contact.
Secure with a secondary dressing (e.g., gauze, non-woven bandage) if needed; adjust fixation based on wound location and exudate volume.
Change the dressing according to wound exudate amount and clinical condition (1-3 days for moderate exudate; daily for heavy exudate/infected wounds) or as directed by a physician.
For Clinical Post-Care (Under Professional Guidance)
Clean the wound with sterile normal saline and dry thoroughly as instructed by a healthcare provider.
Apply the sterile silver ion cotton mesh dressing to cover the entire wound surface.
Secure with a breathable, sterile secondary dressing and avoid tight wrapping that may impede circulation.
Follow the physician’s recommended dressing change schedule; do not reuse the dressing or adjust the application method without professional guidance.
Visuotinis pritaikymas ir atitikties palaikymas
1. Pritaikomos produktų ir pakuočių parinktys

We offer flexible, clinical-grade customization services to meet the unique needs of global distributors, hospitals and wound care centers, with no unnecessary mold costs for standard customizations:

Dressing Customization: Oily/non-oily variants for different exudate levels; custom mesh sizes for specialized clinical use
Sterile Packaging Customization: Medical-grade sealed packaging with multilingual printing (product instructions, brand logo, regulatory marks); custom sterile labels for local clinical standards
Bulk Carton Customization: Branded carton design, batch number/lot code printing, clinical packaging specification adjustment, enhanced transportation protection for long-distance 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

To support seamless local product registration and market access, our professional regulatory team provides a complete set of standardized technical documents that comply with ISO 13485:2016 and regional medical device regulations (EU, Middle East, Southeast Asia, Africa, etc.). All documents are adjustable and supplementable to meet local registration requirements, including but not limited to:

ISO 13485:2016 kokybės vadybos sistemos sertifikavimo dokumentas
Product Technical Specification (TS) with full antibacterial, biocompatibility and performance test data
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
Free document update service: Annual technical document updates to align with revised local regulatory standards

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) Oily/non-oily selection + packaging printing customization (no mold cost) Nemokami pagrindiniai pasaulinės atitikties dokumentai + vertimas į kelias kalbas
Regioniniai klinikiniai platintojai ≥200 dėžių (viena specifikacija) Full customization (dressing size + sterile packaging + carton design) Free localized regulatory documents + registration guidance
Didelės ligoninės / medicinos įstaigos ≥500 dėžių (viena specifikacija) Išskirtinis OEM/ODM + specializuotas klinikinių variantų pritaikymas Nemokami išskirtiniai norminiai dokumentai + specialus registracijos konsultantas + metiniai atnaujinimai
Atsargumo priemonės

1. For external clinical use only; do not use on unhealed deep wounds, severely necrotic wounds or wounds with heavy bleeding without professional physician guidance.

2. Adhere to aseptic technique during application to avoid secondary wound infection; do not reuse the sterile single-use dressing.

3. Discontinue use immediately and consult a physician if the wound shows signs of worsening (e.g., increased redness, swelling, pain, exudate or odor) 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.

5. Do not use the product if the sterile packaging is damaged, torn, 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, cotton, white petrolatum 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, humidity or direct sunlight—may affect silver ion activity and dressing performance.

Kontaktai
Klinikinis verslo bendradarbiavimas ir konsultacijos dėl didmeninių pirkimų
"WhatsApp": https://wa.me/8617788969619 | https://wa.me/8619173969821
Mobilusis / „WeChat“: +86-19173969821 | +86-17788969619
[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 registration document preparation, regulatory compliance guidance
DUK

Q1: What is the difference between the oily and non-oily variants of this silver ion cotton mesh dressing?

A1: The oily variant (infused with white petrolatum/paraffin oil) is designed for low-to-moderate exudate wounds and provides enhanced anti-adhesion for fragile granulation tissue (ideal for ulcers, burns and donor sites). The non-oily variant is optimized for moderate-to-heavy exudate infected wounds, with improved mesh drainage to prevent fluid buildup. Both variants feature the same HBP silver ion sustained release antibacterial technology.

Q2: Can this dressing be cut to fit irregular wound contours (e.g., heel pressure ulcers, facial wounds)?

A2: Yes. The soft medical cotton mesh is easily cut with sterile scissors (aseptic technique required) to custom fit any irregular wound shape or size, with the dressing extending 1-2cm onto healthy skin for full antimicrobial protection. Cutting does not affect the silver ion sustained release performance or the dressing’s structural integrity.

Q3: How long does the HBP silver ion provide antibacterial activity on the wound surface?

A3: The advanced HBP chelation technology enables controlled, sustained silver ion release for up to 72 hours per dressing application, forming a long-lasting antimicrobial barrier on the wound bed. The actual duration may vary slightly based on wound exudate volume—heavier exudate may require more frequent dressing changes to maintain optimal antibacterial efficacy.

Q4: Is this silver ion cotton mesh dressing suitable for diabetic foot ulcers (DFUs)?

A4: Yes. It is a clinical-grade solution for mild-to-moderate infected diabetic foot ulcers with low-to-moderate exudate. The sustained release silver ion technology targets bacterial colonization (a key cause of DFU healing delay), while the anti-adhesion formula minimizes trauma during dressing changes (critical for diabetic skin with reduced circulation). For severe, necrotic or heavily exuding DFUs, use under the direct guidance of a diabetic wound care specialist.

Q5: Can this dressing be used as a secondary dressing for negative pressure wound therapy (NPWT)?

A5: Yes. The non-oily variant is recommended as a contact layer for NPWT for infected wounds with moderate exudate (e.g., surgical wounds, traumatic wounds). It provides a soft, antibacterial contact surface between the NPWT device and the wound bed, preventing tissue ingrowth and maintaining antimicrobial protection during negative pressure therapy. Follow the NPWT device manual and clinical physician guidance for application.

Q6: What storage conditions are required for bulk clinical procurement of this dressing?

A6: Store the sealed cartons in a cool, dry, well-ventilated clinical warehouse with a temperature of 15-25℃ and relative humidity<60%. Avoid direct sunlight, high temperature (>30℃) and humidity (>70%RH) to preserve silver ion activity. Stack cartons on pallets (avoid direct contact with the ground) and follow the "first in, first out" inventory principle; do not stack heavy objects on cartons to prevent packaging damage and loss of sterility.

Q7: Does the dressing require refrigeration for storage or transportation?

A7: No. This silver ion cotton mesh dressing is a room temperature-stable medical device—refrigeration is not required and may cause condensation (which affects packaging sterility). For international transportation (e.g., high-temperature regions like the Middle East), we recommend insulated shipping cartons to avoid prolonged exposure to extreme heat (>40℃), which aligns with our storage condition guidelines.

Q8: Can you provide clinical trial data or case studies for this dressing’s efficacy on chronic ulcers?

A8: Yes. We provide a comprehensive Clinical Validation Report with in vitro antibacterial efficacy data and clinical case studies on venous leg ulcers (VLUs) and pressure ulcers (PUs) (including healing rate, exudate reduction and bacterial clearance data). For global distributors requiring additional clinical evidence for local registration, our R&D team can also provide customized test data and third-party clinical verification reports (per local regulatory requirements).

Q9: What is the lead time for bulk orders and custom packaging?

A9: For standard non-customized bulk orders (oily/non-oily variants, standard sizes), the lead time is 15 working days. For custom packaging/dressing orders (printing, sizes, variants), the lead time is 60 working days (no mold cost for standard customizations). For large hospital/institional bulk orders (≥500 cartons), we offer flexible lead time adjustments and priority production scheduling.

Q10: Do you provide training for clinical staff on the proper application of this dressing?

A10: Yes. For bulk clinical procurement by hospitals/medical institutions, we provide free online clinical application training (conducted by our wound care specialists) covering aseptic application, dressing change techniques, oily/non-oily variant selection and troubleshooting. We also provide a printable clinical application guide (multilingual) for on-site staff training and reference.

TYRIMAS