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BIGopsy

FDA UDI

Class I (US FDA UDI)

by Cook Ireland, Ltd.

Identity

Trade Name
BIGopsy FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
BIGopsy Backloading Biopsy Forceps FDA UDI
Model / Reference
G48240 FDA UDI
Description
BIGopsy Backloading Biopsy Forceps FDA UDI

Identifiers

Catalog Number
BLB-024115 FDA UDI
Primary DI / UDI-DI
10827002482408 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

BIGopsy by Cook Ireland, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Ireland, Ltd.

Sources (1)

  • FDA UDI 0a35b14a-00c9-4aae-8628-fd75fed459c7 36 fields · synced Jun 8, 2026