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MEDRAD Mark V Provis Foot Switch with Cable

FDA UDI

Class II (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name
MEDRAD Mark V Provis Foot Switch with Cable FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
ASSY, CABLE, FOOT SWITCH, UDI, BATCH (86024942)(25 ft.) FDA UDI
Model / Reference
KMA 562-I FDA UDI
Description
ASSY, CABLE, FOOT SWITCH, UDI, BATCH (86024942)(25 ft.) FDA UDI

Identifiers

Catalog Number
KMA 562-I FDA UDI
Primary DI / UDI-DI
00616258020808 FDA UDI
510(k) Number
K903390 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

No

FDA UDI

Category: Foot-switch, electrical

MEDRAD Mark V Provis Foot Switch with Cable by Bayer Medical Care Inc. — Class II — 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 8eac4a3e-70fb-4ede-8a20-e09231b30eea 36 fields · synced Jun 9, 2026