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SINGLE USE BIOPSY VALVE (Sterile)

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
SINGLE USE BIOPSY VALVE (Sterile) FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Device Name
SINGLE USE BIOPSY VALVE MAJ-210 FDA UDI
Model / Reference
MAJ-210 FDA UDI
Description
SINGLE USE BIOPSY VALVE MAJ-210 FDA UDI

Identifiers

Catalog Number
GL2167 FDA UDI
Primary DI / UDI-DI
14953170152433 FDA UDI
FDA Product Code
EOB FDA UDI
EOQ FDA UDI
NWB FDA UDI
GMDN Term
Endoscope working-channel valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 FDA UDI
874.4680 FDA UDI
876.1500 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

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: Endoscope working-channel valve, single-use

SINGLE USE BIOPSY VALVE (Sterile) by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope working-channel valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 387718f4-50f4-41b0-a129-211462cf1503 35 fields · synced May 30, 2026