Identity
- Trade Name
- Dubois Twistripper (set) FDA UDI
- Generic Name
- Vein stripper, reusable FDA UDI
- Device Name
- Surgical instruments for varicose extraction (200 & 300 mm) FDA UDI
- Model / Reference
- A1-350 FDA UDI
- Description
- Surgical instruments for varicose extraction (200 & 300 mm) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20697660005700 FDA UDI
- FDA Product Code
- GAI FDA UDI
- GMDN Term
- Vein stripper, 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
Yes
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
Dubois Twistripper (set) 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 5d584fb4-3e86-4345-aa21-818bc5d9aaff 35 fields · synced May 30, 2026