Identity
- Trade Name
- VEGA FDA UDI
- Generic Name
- Surgical cutting/shaping board, reusable FDA UDI
- Device Name
- VEGA A/P 4-IN-1 CUTTING BLOCK F7 FDA UDI
- Model / Reference
- MF192R FDA UDI
- Description
- VEGA A/P 4-IN-1 CUTTING BLOCK F7 FDA UDI
Identifiers
- Catalog Number
- MF192R FDA UDI
- Primary DI / UDI-DI
- 04046955256662 FDA UDI
- FDA Product Code
- HTZ FDA UDI
- GMDN Term
- Surgical cutting/shaping board, 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
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
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
Vega by Aesculap Implant Systems, 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
- Aesculap Implant Systems, Inc.
Sources (1)
- FDA UDI 70dbb9e4-f1d8-4c0e-9f2f-b9e5e00f5d30 36 fields · synced May 30, 2026