Identity
- Trade Name
- VENAPAX XL FDA UDI
- Generic Name
- Flexible endoscopic scissors, reusable FDA UDI
- Model / Reference
- VPX4000 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888233078986 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Flexible endoscopic scissors, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Flexible endoscopic scissors, reusable
Venapax Xl by Biomet Microfixation, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Flexible endoscopic scissors, reusable.
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- ELMED — ELMED INCORPORATED · Class I
- Gyrus ACMI — Gyrus Acmi, Inc. · Class I
- ELMED — ELMED INCORPORATED · Class I
- HYSAFE — Richard Wolf GmbH · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Biomet Microfixation, Inc
Sources (1)
- FDA UDI 8a832436-2109-41f2-ba31-00064f784d61 32 fields · synced May 30, 2026