Identity
- Trade Name
- OsteoMed FDA UDI
- Generic Name
- Surgical countersink, single-use FDA UDI
- Device Name
- Ø2.7mm Drill/Cntrsnk Cmbo Long, Quick Release FDA UDI
- Model / Reference
- 316-0548 FDA UDI
- Description
- Ø2.7mm Drill/Cntrsnk Cmbo Long, Quick Release FDA UDI
Identifiers
- Catalog Number
- 316-0548 FDA UDI
- Primary DI / UDI-DI
- 00842528126424 FDA UDI
- FDA Product Code
- HTW FDA UDI
- GMDN Term
- Surgical countersink, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 24 Millimeter FDA UDI
Category: Surgical countersink, single-use
OsteoMed by Osteomed Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- FuzeFix Mini — FUSION ORTHOPEDICS, LLC · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Osteomed Corp.
Sources (1)
- FDA UDI 263d4af5-7cdd-41ac-adc8-1b9aeb75df43 37 fields · synced May 30, 2026