Medical Biological Polysaccharide Wound Repair Dressing
Type I: Indicated for the care of non-chronic wounds (such as superficial wounds, postoperative sutured wounds, mechanical trauma, first-degree or superficial second-degree burn wounds, and wounds after laser/photon/alpha-hydroxy acid peeling/microplastic surgery), providing a microenvironment for wound healing. Type II, III, IV: Indicated for the care of superficial wounds such as small wounds, abrasions, and cuts, as well as the surrounding skin, providing...
Type I: Indicated for the care of non-chronic wounds (such as superficial wounds, postoperative sutured wounds, mechanical trauma, first-degree or superficial second-degree burn wounds, and wounds after laser/photon/alpha-hydroxy acid peeling/microplastic surgery), providing a microenvironment for wound healing. Type II, III, IV: Indicated for the care of superficial wounds such as small wounds, abrasions, and cuts, as well as the surrounding skin, providing a microenvironment for wound healing. The Medical Biological Polysaccharide Wound Repair Dressing is available in four models: Type I, Type II, Type III, and Type IV. Type I consists of liquid and non-woven fabric film, packaged in aluminum foil bags; Type II consists of liquid and glass bottles; Type III consists of liquid and plastic bottles (Pt material); Type IV consists of liquid and borosilicate glass tubes. The liquid of this product is composed of Carbomer, Sodium Hyaluronate, Butylene Glycol, Glycerin, Hydroxyacetophenone, 1,2-Hexanediol, Ectoine, Triethanolamine, Xanthan Gum, Disodium Edetate, and Purified Water. The product is sterilized by moist heat and supplied sterile.
MOQ
—
Sample Lead Time
7–14 days
Production Lead Time
25–35 days
Service Modes
OEM · ODM · Private Label
Specifications / Attributes
- National Class II Medical Device Registration Certificate (Hunan Medical Device Registration)
- Main Ingredients: Carbomer, Sodium Hyaluronate, Butylene Glycol, Glycerin, Hydroxyacetophenone, 1,2-Hexanediol, Ectoine, Triethanolamine, Xanthan Gum, Disodium Edetate, Purified Water
- Sterile Supply (Irradiation Sterilization)
- Supports custom OEM/ODM specifications and packaging
Technical Specifications
- Registration No.: Xiang Medical Device Registration 20242140153
- Model: Aluminum Foil Bag (Type I), Glass Bottle (Type II), Plastic Bottle (Type III), Glass Tube (Type IV)
- Packaging: Type I, Type II, Type III, Type IV
- Sterility: Sterile Supply
Why Weitai
Why Choose Weitai?
Dual cosmetics & medical device expertise — full-chain control from formula to mass production.
Process
How We Work
Six standardized steps from idea to market, fully under control.
Requirement Discovery
Define product type, specs, quantity, target market and compliance.
Formulation & Sampling
R&D team develops custom formulas and provides samples for review.
Confirmation & Quote
Confirm formula, packaging & MOQ, sign cooperation agreement.
Mass Production & QC
Produce under GMP with full quality monitoring throughout.
Filling & Labeling
Filling, packaging and private-label per brand requirements.
Delivery & Release
Outgoing inspection, compliance documentation and logistics.
Compliance
Certifications & Qualifications
Dual expertise keeps your brand compliant in every target market.
Packaging
Packaging Options
Multiple packaging formats with full customization.
Bottle
瓶
Tube
管
Jar
罐
Ampoule
安瓿
Lyophilized Dual-Chamber
冻干双腔
Mask Sachet
面膜袋
FAQ
FAQ
Everything you may want to know about manufacturing, sampling and compliance.
What is your minimum order quantity (MOQ)?+
MOQ varies by product. Medical gels and dressings generally start from 10,000 units, while skin care can be lower. It depends on the product and formula—please contact us for a quote.
What certifications does Weitai Group hold?+
Weitai Group is fully qualified: certified with ISO13485 (medical device quality management) and ISO22716/GMPC (cosmetics GMP), recognized as a National High-Tech Enterprise, and certified with GB/T29490 IP management system. We hold 110+ Class II medical device registrations, 72 invention patents and 30+ international patents, operate 100,000-class GMP cleanrooms across six production bases totaling 150,000 m² with 65 automated production lines, and bring 25+ years of OEM/ODM experience serving 1000+ partner brands.
What is the difference between ODM and OEM?+
OEM manufactures your existing formulas and machines under your brand; ODM offers full customization from formula development, packaging design to registration. Weitai supports both and provides free formula development and documentation kits.
Can you provide formula development?+
Yes. With a 105-person R&D team, Weitai offers free formula development, packaging design, and documentation kits (brochures, detail pages, test reports) plus assistance with registration.
How can I get a quote?+
Please submit your product requirements and quantities via the inquiry form or sales@zhenmeifu.com. Our dedicated sales will contact you within 24 hours with a proposal and quotation.
Can you provide OEM/ODM contract manufacturing for PLLA microsphere injectable fillers?+
Yes. Weitai supports OEM/ODM contract manufacturing for Class III Medical Device injectable filler products, including PLLA microsphere injectable fillers. The microspheres feature uniform and controllable particle size and are biodegradable, with customizable formulations and aseptic filling available.
Turn your product idea into reality
Bring your product idea to a reliable partner — from formula and sample to mass production, Weitai walks with you end to end.