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Competitive Precision Micro Premium Blade for ConMed®/Linvatec® Hall®
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Competitive Precision Micro Premium Blade for ConMed®/Linvatec® Hall® FDA UDI
- Generic Name
- Surgical saw blade, sagittal, single-use FDA UDI
- Model / Reference
- CM700-070-150P FDA UDI
Identifiers
- Catalog Number
- CM700-070-150P FDA UDI
- Primary DI / UDI-DI
- 14053613292723 FDA UDI
- FDA Product Code
- GFA FDA UDI
- GMDN Term
- Surgical saw blade, sagittal, single-use 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical saw blade, sagittal, single-use
Competitive Precision Micro Premium Blade for ConMed®/Linvatec® Hall® by Gebr. Brasseler GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Surgical saw blade, sagittal, single-use.
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- IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
- IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
- IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
- Arthrex® — Arthrex, Inc. · 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 e4b1bbcd-16f3-4e19-8c93-7470d0e472eb 33 fields · synced May 30, 2026