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Footswitch for SONICBEAT

FDA UDI

Class U (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Footswitch for SONICBEAT FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Model / Reference
MAJ-1869 FDA UDI

Identifiers

Catalog Number
N3809130 FDA UDI
Primary DI / UDI-DI
04953170308390 FDA UDI
510(k) Number
K111202 FDA UDI
FDA Product Code
LFL FDA UDI
GEI FDA UDI
KNS FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
878.4400 FDA UDI
876.4300 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

Footswitch for SONICBEAT by Olympus Medical Systems Corporation — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2f23befb-e697-4a75-9409-71377b5bae62 35 fields · synced Jun 8, 2026