Identity
- Trade Name
- COLUMBUS FDA UDI
- Generic Name
- Surgical cutting/shaping board, reusable FDA UDI
- Device Name
- IQ COLUMBUS A/P 4-IN-1 CUTTING GUIDE F3 FDA UDI
- Model / Reference
- MF217R FDA UDI
- Description
- IQ COLUMBUS A/P 4-IN-1 CUTTING GUIDE F3 FDA UDI
Identifiers
- Catalog Number
- MF217R FDA UDI
- Primary DI / UDI-DI
- 04046955256686 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
Columbus 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 12dd9585-9932-429f-8b74-809358a41eac 36 fields · synced Jun 6, 2026