Identity
- Trade Name
- cofoe FDA UDI
- Generic Name
- Synthetic-polymer liquid barrier dressing FDA UDI
- Device Name
- Skin Barrier Wipe FDA UDI
- Model / Reference
- C1 FDA UDI
- Description
- Skin Barrier Wipe FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06950715505618 FDA UDI
- FDA Product Code
- EXE FDA UDI
- GMDN Term
- Synthetic-polymer liquid barrier dressing FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5900 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
No
FDA UDI
Over-the-Counter
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Synthetic-polymer liquid barrier dressing
cofoe by Cofoe Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Synthetic-polymer liquid barrier dressing.
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- SECURA No-Sting Barrier Film Wipes Bulk — Smith & Nephew Medical, Ltd. · Class I
- Sting Free — DERMARITE INDUSTRIES LLC · Class I
- 3M™ Cavilon™ — 3M COMPANY · Class I
- ProCure — Twin Med, LLC · 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 |
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Manufacturer
- Manufacturer
- Cofoe Medical Technology Co., Ltd.
Sources (1)
- FDA UDI 1f8055cb-74c9-48e3-9de2-69a154cfb7e6 33 fields · synced May 30, 2026