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Gas/Water Valve

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
GAS/WATER VALVE FDA UDI
Generic Name
Endoscope air/water valve, reusable FDA UDI
Model / Reference
MAJ-2010 FDA UDI

Identifiers

Catalog Number
N4456731 FDA UDI
Primary DI / UDI-DI
04953170437830 FDA UDI
FDA Product Code
FDF FDA UDI
GMDN Term
Endoscope air/water valve, reusable 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

No

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 air/water valve, reusable

Gas/Water Valve by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope air/water valve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b96ea3e-676b-404c-98f2-0fbc848580b5 34 fields · synced May 30, 2026