Identity
- Trade Name
- CONMED FDA UDI
- Generic Name
- Laparoscopic insufflator FDA UDI
- Device Name
- 50L ABDOMINAL INSUFFLATOR FDA UDI
- Model / Reference
- GS2000 FDA UDI
- Description
- 50L ABDOMINAL INSUFFLATOR FDA UDI
Identifiers
- Catalog Number
- GS2000 FDA UDI
- Primary DI / UDI-DI
- 10845854045398 FDA UDI
- FDA Product Code
- HIF FDA UDI
- GMDN Term
- Laparoscopic insufflator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1730 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Laparoscopic insufflator
Conmed by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laparoscopic insufflator.
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- High pressure tube CO2 DIN:US — W.O.M. World of Medicine GmbH · Class I
- CO2 gas connecter, angled — W.O.M. World of Medicine GmbH · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 56f4f06f-1076-4a77-9370-f6a3700912f0 36 fields · synced Jun 1, 2026