Identity
- Trade Name
- MICROCHOICE FDA UDI
- Generic Name
- Sternum saw blade, single-use FDA UDI
- Device Name
- MICROCHOICE REPEAT STERNOTOMY BLADE 65.8 MM FDA UDI
- Model / Reference
- 00502318000 FDA UDI
- Description
- MICROCHOICE REPEAT STERNOTOMY BLADE 65.8 MM FDA UDI
Identifiers
- Catalog Number
- 5023-180 FDA UDI
- Primary DI / UDI-DI
- 10845854006160 FDA UDI
- FDA Product Code
- GFA FDA UDI
- GMDN Term
- Sternum saw blade, 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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 65.8 Millimeter FDA UDI
Category: Sternum saw blade, single-use
Microchoice by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Conmed Corporation
Sources (1)
- FDA UDI a7cf9c15-f6d4-44fe-aaf4-d4743f92b27a 36 fields · synced May 30, 2026