Identity
- Trade Name
- SYSTEM 5000 FDA UDI
- Generic Name
- Electrosurgical system generator FDA UDI
- Device Name
- ELECTROSURGICAL APPARATUS, SYSTEM 5000 USM KIT FDA UDI
- Model / Reference
- 60-8005-USM FDA UDI
- Description
- ELECTROSURGICAL APPARATUS, SYSTEM 5000 USM KIT FDA UDI
Identifiers
- Catalog Number
- 60-8005-USM FDA UDI
- Primary DI / UDI-DI
- 20845854045579 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrosurgical system generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electrosurgical system generator
System 5000 by Conmed Corporation — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (2)
- FDA UDI bb314c02-7b40-47de-9bbd-a0ec37c2db59 36 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced May 28, 2026