Identity
- Trade Name
- Kumar Clamp® FDA UDI
- Generic Name
- Laparoscopic tissue manipulation forceps/working-channel FDA UDI
- Device Name
- The Kumar Clamp® is a reusable 5mm stainless steel laparoscopic grasper of 37 cm length with long ( 3.8 cm) atraumatic jaws and a channel for introduction of the single use Kumar Catheter®. The system is meant to provide a method of laparoscopic cholangiography. FDA UDI
- Model / Reference
- KC-002 FDA UDI
- Description
- The Kumar Clamp® is a reusable 5mm stainless steel laparoscopic grasper of 37 cm length with long ( 3.8 cm) atraumatic jaws and a channel for introduction of the single use Kumar Catheter®. The system is meant to provide a method of laparoscopic cholangiography. FDA UDI
Identifiers
- Catalog Number
- KC-002 FDA UDI
- Primary DI / UDI-DI
- B361KC0020 FDA UDI
- 510(k) Number
- K973621 FDA UDI
- FDA Product Code
- GBZ FDA UDI
- GMDN Term
- Laparoscopic tissue manipulation forceps/working-channel FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 5 Millimeter FDA UDILength — 37 Centimeter FDA UDI
Category: Laparoscopic tissue manipulation forceps/working-channel
Kumar Clamp® by Nashville Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Nashville Surgical Instruments
Sources (1)
- FDA UDI 904e21e2-5e41-40c9-9cd6-ab719b633a68 37 fields · synced May 30, 2026