Identity
- Trade Name
- LAP CHOLE W/CLIP APPLIER FDA UDI
- Generic Name
- Laparoscopic access cannula, single-use FDA UDI
- Device Name
- Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX C2201, 120MM INSUFF NEEDLE XE, 20/BX CTF03, 5x100 Kii® Fios® Z-THR 6/BX CTF33, 11x100 Kii® Fios® ZTHR 6/BX CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX FDA UDI
- Model / Reference
- K2212 FDA UDI
- Description
- Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX C2201, 120MM INSUFF NEEDLE XE, 20/BX CTF03, 5x100 Kii® Fios® Z-THR 6/BX CTF33, 11x100 Kii® Fios® ZTHR 6/BX CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30607915127504 FDA UDI
- FDA Product Code
- HET FDA UDIGCJ FDA UDIFZP FDA UDIMDM FDA UDI
- GMDN Term
- Laparoscopic access cannula, single-use FDA UDI
Classification
- Device Class
- Class II 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-useSpring-loaded pneumoperitoneum needle, single-use
Lap Chole W/Clip Applier by Applied Medical Resources Corp. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
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Also classified as Spring-loaded pneumoperitoneum needle, single-use.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K964470 | Class II | Active |
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Manufacturer
- Manufacturer
- Applied Medical Resources Corp.
- FDA Applicant
- Applied Medical Resources
Sources (2)
- FDA UDI 015bff20-a9e0-475b-9576-aaa60db29438 58 fields · synced Jun 18, 2026
- FDA 510(k) K964470 1 fields · synced May 25, 2026