Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Orthopaedic osteotome FDA UDI
- Device Name
- HEXAGONAL HANDLE OSTEOTOME BLADE 4MM WIDE OVERALL LENGTH 6-1/4 inches15.9CM FDA UDI
- Model / Reference
- RH1465-4 FDA UDI
- Description
- HEXAGONAL HANDLE OSTEOTOME BLADE 4MM WIDE OVERALL LENGTH 6-1/4 inches15.9CM FDA UDI
Identifiers
- Catalog Number
- RH14654 FDA UDI
- Primary DI / UDI-DI
- 10885403112959 FDA UDI
- FDA Product Code
- KAN FDA UDI
- GMDN Term
- Orthopaedic osteotome FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
Category: Orthopaedic osteotome
V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic osteotome.
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- gSource — GSOURCE, LLC. · Class I
- INSTRUMENT — Howmedica Osteonics Corp. · Class I
- ORTHOMED — ORTHO-MED, INC. · Class I
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
- Steris Corporation
Sources (1)
- FDA UDI 12145157-ae71-42bc-b803-5240aa4642ec 35 fields · synced Jun 8, 2026