Identity
- Trade Name
- LAP CHOLE KIT DR. WEHMAN FDA UDI
- Generic Name
- Tissue extraction bag FDA UDI
- Device Name
- Kit Contains: CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX CTR03, 5x100 Kii® OPT ZTHR 6/BX CTS12, 11x100 Kii® SLEEVE ZTHR 12/BX CTR33, 11X100 Kii® OPT ZTHR 6/BX CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BX C4119, 32CM GRASPER REPOS CART, 10/BX CB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX FDA UDI
- Model / Reference
- K2153 FDA UDI
- Description
- Kit Contains: CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX CTR03, 5x100 Kii® OPT ZTHR 6/BX CTS12, 11x100 Kii® SLEEVE ZTHR 12/BX CTR33, 11X100 Kii® OPT ZTHR 6/BX CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BX C4119, 32CM GRASPER REPOS CART, 10/BX CB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30607915133956 FDA UDI
- FDA Product Code
- NWV FDA UDIHET FDA UDIGCJ FDA UDIFZP FDA UDIMDM FDA UDI
- GMDN Term
- Tissue extraction bag 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
Lap Chole Kit Dr. Wehman 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 4064b68e-eccf-4644-859b-2b13c938acaa 34 fields · synced Jun 1, 2026