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Biopsy Valve

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Biopsy Valve FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Device Name
"MAJ-853 Biopsy valves 140-AL5/160-OL5" FDA UDI
Model / Reference
MAJ-853 FDA UDI
Description
"MAJ-853 Biopsy valves 140-AL5/160-OL5" FDA UDI

Identifiers

Catalog Number
N5363700 FDA UDI
Primary DI / UDI-DI
04953170355943 FDA UDI
FDA Product Code
ODG FDA UDI
GMDN Term
Endoscope working-channel valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscope working-channel valve, single-use

Biopsy Valve 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 e3daa2b2-4397-408d-871a-7703e4afc295 35 fields · synced May 30, 2026