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Sonicweld Rx

FDA UDI

Class II (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
SONICWELD RX FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
FOOTSWITCH, CIRCULAR, W/CABLE FDA UDI
Model / Reference
52-500-02-04 FDA UDI
Description
FOOTSWITCH, CIRCULAR, W/CABLE FDA UDI

Identifiers

Primary DI / UDI-DI
00888118084866 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Foot-switch, electrical

Sonicweld Rx by KLS-Martin L.P. — 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

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI a2dd955d-831e-4348-a0a9-187bad364b59 34 fields · synced Jun 1, 2026