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Skin Hook Retractor (with 2 Sharp Prongs) (non glare)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Skin Hook Retractor (with 2 Sharp Prongs) (non glare) FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- The Skin Hook is a retractor with two sharp prongs. All non-reflective. FDA UDI
- Model / Reference
- 28-012 FDA UDI
- Description
- The Skin Hook is a retractor with two sharp prongs. All non-reflective. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10697660003747 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Skin Hook Retractor (with 2 Sharp Prongs) (non glare) by Oculo-Plastik Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Oculo-Plastik Inc
Sources (1)
- FDA UDI e328fe2a-82cc-4127-ba3d-dcff8843fb4f 35 fields · synced May 30, 2026