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Dr. Bhuta Lap Chole

FDA UDI

Class II (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name
DR. BHUTA LAP CHOLE FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CTB03, 5x100 Kii® SH BLD ZTHR 6/BX CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CTB73, 12x100 Kii® SH BLD ZTHR 6/BX C4120, 38CM GRASPER REPOS CART, 10/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX FDA UDI
Model / Reference
K2741 FDA UDI
Description
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CTB03, 5x100 Kii® SH BLD ZTHR 6/BX CTS02, 5x100 Kii® SLEEVE ZTHR 12/BX C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CTB73, 12x100 Kii® SH BLD ZTHR 6/BX C4120, 38CM GRASPER REPOS CART, 10/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX FDA UDI

Identifiers

Primary DI / UDI-DI
30607915134380 FDA UDI
FDA Product Code
HET FDA UDI
NWV FDA UDI
GCJ FDA UDI
FZP FDA UDI
MDM FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 FDA UDI
876.1500 FDA UDI
878.4300 FDA UDI
878.4800 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. Bhuta Lap Chole by Applied Medical Resources Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic grasping forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Medical Resources Corp.

Sources (1)

  • FDA UDI 13a0d68e-ca46-43e5-b4e6-b8d25915697b 34 fields · synced May 30, 2026