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Smoke Evacuation Foot Switch

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
SMOKE EVACUATION FOOT SWITCH FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
MAJ-1939 SMOKE EVACUATION FOOT SWITCH FDA UDI
Model / Reference
MAJ-1939 FDA UDI
Description
MAJ-1939 SMOKE EVACUATION FOOT SWITCH FDA UDI

Identifiers

Primary DI / UDI-DI
04953170324185 FDA UDI
FDA Product Code
HIF FDA UDI
OSV FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

Smoke Evacuation Foot Switch by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9c99390-a4c4-400f-9fb0-5699e4da13c5 34 fields · synced Jun 8, 2026