Identity
- Trade Name
- Cofoe FDA UDI
- Generic Name
- Wrist orthosis FDA UDI
- Device Name
- Wrist Brace FDA UDI
- Model / Reference
- KF-GDD-F04 FDA UDI
- Description
- Wrist Brace FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06950715501696 FDA UDI
- FDA Product Code
- ILH FDA UDI
- GMDN Term
- Wrist orthosis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3475 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: Wrist orthosis
Cofoe by Cofoe Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wrist orthosis.
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- MEDI — MEDI MANUFACTURING, INC. · Class I
- PROCARE — DJO, LLC · Class I
- Push Sports — Nea International B.V. · Class I
- Wrist Lacer — MEDICAL SPECIALTIES INCORPORATED · Class I
- MEDI — MEDI MANUFACTURING, INC. · 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 5d5d8dea-141c-446c-ae01-e3f360da6c1e 34 fields · synced May 30, 2026