Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Surgical saw blade, reciprocating, reusable FDA UDI
- Device Name
- SAW BLADE F/GB130R/GB391R 33/0.4/0.6 RT FDA UDI
- Model / Reference
- GC926R FDA UDI
- Description
- SAW BLADE F/GB130R/GB391R 33/0.4/0.6 RT FDA UDI
Identifiers
- Catalog Number
- GC926R FDA UDI
- Primary DI / UDI-DI
- 04046963130350 FDA UDI
- FDA Product Code
- GEY FDA UDI
- GMDN Term
- Surgical saw blade, reciprocating, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical saw blade, reciprocating, reusable
Aesculap by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical saw blade, reciprocating, reusable.
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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
- Aesculap, Inc.
Sources (1)
- FDA UDI c4ac6018-52a9-4e7b-903a-5519a156bdbe 35 fields · synced May 30, 2026