Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Surgical saw blade, oscillating, reusable FDA UDI
- Device Name
- SAW BLADE S SAGITTAL 15/5/0.3MM FDA UDI
- Model / Reference
- GP492R FDA UDI
- Description
- SAW BLADE S SAGITTAL 15/5/0.3MM FDA UDI
Identifiers
- Catalog Number
- GP492R FDA UDI
- Primary DI / UDI-DI
- 04046964643002 FDA UDI
- FDA Product Code
- HBE FDA UDIGEY FDA UDI
- GMDN Term
- Surgical saw blade, oscillating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4310 FDA UDI878.4820 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Aesculap by Aesculap, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 44710020-c405-4a29-a09a-9b09c3269229 36 fields · synced Jun 1, 2026