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FUJIFILM medwork

FDA UDI

Class II (US FDA UDI)

by FUJIFILM medwork GmbH

Identity

Trade Name
FUJIFILM medwork FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Model / Reference
VAL1-G7-4-50-1 FDA UDI

Identifiers

Catalog Number
VAL1-G7-4-50-1 FDA UDI
Primary DI / UDI-DI
04044503002341 FDA UDI
FDA Product Code
ODC FDA UDI
FDF FDA UDI
FPA 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
880.5440 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Endoscope working-channel valve, single-useEndoscope suction valve, single-useEndoscope air/water valve, single-useIn-line backflow valve, single-use

FUJIFILM medwork by FUJIFILM medwork GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as In-line backflow valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af804fe9-381f-4efe-8964-597f16b60744 34 fields · synced Jun 6, 2026