Identity
- Trade Name
- Periosteal Elevator, Straight, 12mm Tip, 7.5cm WL FDA UDI
- Generic Name
- Bone lever/elevator, reusable FDA UDI
- Device Name
- Elevator FDA UDI
- Model / Reference
- 99-400-45 FDA UDI
- Description
- Elevator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810009465416 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Bone lever/elevator, 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
No
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
Periosteal Elevator, Straight, 12mm Tip, 7.5cm WL by Mizuho America, 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
- Mizuho America, Inc.
Sources (1)
- FDA UDI d6bf2870-41ff-4ade-8b9f-e024fd4a7ebb 34 fields · synced May 30, 2026