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Suction Valve

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Suction Valve FDA UDI
Generic Name
Endoscope working-channel valve, reusable FDA UDI
Device Name
"MD-493 SUCTION VALVE FOR BF-20 /ENF-T3" FDA UDI
Model / Reference
MD-493 FDA UDI
Description
"MD-493 SUCTION VALVE FOR BF-20 /ENF-T3" FDA UDI

Identifiers

Catalog Number
GX0366 FDA UDI
Primary DI / UDI-DI
04953170064104 FDA UDI
FDA Product Code
FDS FDA UDI
EOB FDA UDI
GMDN Term
Endoscope working-channel valve, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
874.4760 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, reusable

Suction 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, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI e67c41c1-f03d-44a8-b165-555d1e7d2ca9 35 fields · synced May 30, 2026