Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Bone file/rasp, manual, reusable FDA UDI
- Device Name
- V. Mueller ORAL BONE FILE DOUBLE-ENDED, SERRATED ENDS 20 X 5MM & 12 X 3MM WIDE OVERALL LENGTH 7-1/4" (18.4CM) FDA UDI
- Model / Reference
- MO10055 FDA UDI
- Description
- V. Mueller ORAL BONE FILE DOUBLE-ENDED, SERRATED ENDS 20 X 5MM & 12 X 3MM WIDE OVERALL LENGTH 7-1/4" (18.4CM) FDA UDI
Identifiers
- Catalog Number
- MO10055 FDA UDI
- Primary DI / UDI-DI
- 10885403068645 FDA UDI
- FDA Product Code
- EMI FDA UDI
- GMDN Term
- Bone file/rasp, manual, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
V. Mueller by Carefusion 2200, 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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI c44c084a-c477-431f-ba7a-5a02e04d24b8 36 fields · synced Sep 18, 2026