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Dr. Barry

FDA UDI

Class I (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name
DR. BARRY FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CFF03, 5x100 Kii® Fios® ADVFIX 6/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CFR73, 12x100 Kii® OPT ADVFIX 6/BX CFB73, 12x100 Kii® SH BLD ADVFIX 6/BX C4120, 38CM GRASPER REPOS CART, 10/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX FDA UDI
Model / Reference
K2737 FDA UDI
Description
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CFF03, 5x100 Kii® Fios® ADVFIX 6/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CFR73, 12x100 Kii® OPT ADVFIX 6/BX CFB73, 12x100 Kii® SH BLD ADVFIX 6/BX C4120, 38CM GRASPER REPOS CART, 10/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX FDA UDI

Identifiers

Primary DI / UDI-DI
30607915134397 FDA UDI
FDA Product Code
NWV FDA UDI
GCJ FDA UDI
HET FDA UDI
FZP FDA UDI
MDM FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class I 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. Barry 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.

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 1595d58b-9b15-4dfe-9243-b8d68d420ad3 34 fields · synced May 31, 2026