Identity
- Trade Name
- KOMET Surgical Saw Blade FDA UDI
- Generic Name
- Bone file/rasp, reciprocating, reusable FDA UDI
- Model / Reference
- KM37116. ST..M1 FDA UDI
Identifiers
- Catalog Number
- KM37116. ST. FDA UDI
- Primary DI / UDI-DI
- 14053613176559 FDA UDI
- FDA Product Code
- GFA FDA UDI
- GMDN Term
- Bone file/rasp, 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
Yes
FDA UDI
Category: Bone file/rasp, reciprocating, reusable
KOMET Surgical Saw Blade by Gebr. Brasseler GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- KOMET Surgical Saw Blade — Gebr. Brasseler GmbH & Co. KG · 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
- Gebr. Brasseler GmbH & Co. KG
Sources (1)
- FDA UDI be9e8ea2-a0a4-455f-bbe2-85c044f0cf62 33 fields · synced Jun 8, 2026