← Back to catalogue

Single Use Biopsy Forceps

FDA UDI

Class I (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Single Use Biopsy Forceps FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Model / Reference
FB-245U FDA UDI

Identifiers

Catalog Number
N5998731 FDA UDI
Primary DI / UDI-DI
04953170458040 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

No

FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Single Use Biopsy Forceps by Olympus Medical Systems Corporation — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1e0cde9c-95ed-4c51-ab4d-e0c41fcfa771 34 fields · synced Jun 8, 2026