Identity
- Trade Name
- GARG FDA UDI
- Generic Name
- General surgical procedure kit, medicated FDA UDI
- Device Name
- GARG THORACENTESIS NEEDLE KIT FDA UDI
- Model / Reference
- Kit-1720 FDA UDI
- Description
- GARG THORACENTESIS NEEDLE KIT FDA UDI
Identifiers
- Catalog Number
- Kit-1720 FDA UDI
- Primary DI / UDI-DI
- 20653405058264 FDA UDI
- 510(k) Number
- K894326 FDA UDI
- FDA Product Code
- GAA FDA UDI
- GMDN Term
- General surgical procedure kit, medicated FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
No
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
- Outer Diameter — 2.3 Millimeter FDA UDILength — 8 Centimeter FDA UDI
Garg by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 28969fc8-0068-4607-8d87-a26e3e1c82bf 38 fields · synced May 30, 2026