Identity
- Trade Name
- Anscare Scar Reduction Silicone Gel C+ FDA UDI
- Generic Name
- Scar-management dressing, single-use FDA UDI
- Device Name
- Anscare Scar Reduction Silicone Gel C+ helps prevent and treat both existing and new scars like keloids and hypertrophic scars resulting from surgery, trauma, burns, etc. (External Use Only) FDA UDI
- Model / Reference
- SC201-2 FDA UDI
- Description
- Anscare Scar Reduction Silicone Gel C+ helps prevent and treat both existing and new scars like keloids and hypertrophic scars resulting from surgery, trauma, burns, etc. (External Use Only) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 14719745504324 FDA UDI
- FDA Product Code
- MDA FDA UDI
- GMDN Term
- Scar-management dressing, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4025 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Scar-management dressing, single-use
Anscare Scar Reduction Silicone Gel C+ by Benq Materials Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Scar-management dressing, single-use.
- ScarAway Silicone Acne Scar Gel — ALLIANCE PHARMA INC. · Class I
- H&H — TRONJEN MEDICAL TECHNOLOGY INC. · Class I
- Kelo-cote Advanced Formula Scar Gel — ALLIANCE PHARMA INC. · Class I
- NewGel+UV Silicone Gel for Scars + SPF30 — Newmedical Technology, Inc. · Class I
- NEW BEGINNINGS® GELSHAPES® — Pmt Corp. · Class I
- ScarMD — AIM MEDICAL INC · Class I
- ScarAway Silicone Scar Gel — ALLIANCE PHARMA INC. · Class I
- Lorski — Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Benq Materials Corp.
Sources (1)
- FDA UDI b1b87ade-2cc1-4bae-b8d4-91f97cda8684 33 fields · synced May 30, 2026