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Washing Tube

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
WASHING TUBE FDA UDI
Generic Name
Luminal device flushing tubing set, reusable FDA UDI
Device Name
"MH-974 CLEANING ADPTR- EVIS/OES 100/130" FDA UDI
Model / Reference
MH-974 FDA UDI
Description
"MH-974 CLEANING ADPTR- EVIS/OES 100/130" FDA UDI

Identifiers

Catalog Number
GV442400 FDA UDI
Primary DI / UDI-DI
04953170071362 FDA UDI
FDA Product Code
FET FDA UDI
GMDN Term
Luminal device flushing tubing set, 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

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: Luminal device flushing tubing set, reusable

Washing Tube by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luminal device flushing tubing set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 60f3f9a4-ceaa-4435-b1de-19ae7aef0f1f 35 fields · synced May 30, 2026