Identity
- Trade Name
- DR. GARY LAP CHOLE FDA UDI
- Generic Name
- Rigid endoscopic grasping forceps, single-use FDA UDI
- Device Name
- Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CFB03, 5x100 Kii® SH BLD ADVFIX, 6/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX C4120, 38CM GRASPER REPOS CART, 10/BX CTB73, 12x100 Kii® SH BLD ZTHR 6/BX FDA UDI
- Model / Reference
- K2738 FDA UDI
- Description
- Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CFB03, 5x100 Kii® SH BLD ADVFIX, 6/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX C4120, 38CM GRASPER REPOS CART, 10/BX CTB73, 12x100 Kii® SH BLD ZTHR 6/BX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30607915134359 FDA UDI
- FDA Product Code
- NWV FDA UDIHET FDA UDIGCJ FDA UDIFZP FDA UDIMDM FDA UDI
- GMDN Term
- Rigid endoscopic grasping forceps, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.1720 FDA UDI876.1500 FDA UDI878.4300 FDA UDI878.4800 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ligation clip, metallicLaparoscopic access cannula, single-useEndoscopic electrosurgical handpiece/electrode, monopolar, single-useTissue extraction bag
Dr. Gary Lap Chole by Applied Medical Resources Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic grasping forceps, single-use.
- Endoch — Endoch Inc · Class I
- Endoch — Endoch Inc · Class II
- Endoch — Endoch Inc · Class I
- Endoch — Endoch Inc · Class II
- Endoch — Endoch Inc · Class I
- Endoch — Endoch Inc · Class I
- Endoch — Endoch Inc · Class II
- Endoch — Endoch Inc · Class II
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
- Applied Medical Resources Corp.
Sources (1)
- FDA UDI 5247f9cc-8e36-42cf-9c3a-88c4d983299e 34 fields · synced May 31, 2026