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LithoClast

FDA UDI

Class II (US FDA UDI)

by E.M.S. Electro Medical Systems S.A.

Identity

Trade Name
LithoClast FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
Foot pedal LithoClast Master Refurbished FDA UDI
Model / Reference
EK-166BR FDA UDI
Description
Foot pedal LithoClast Master Refurbished FDA UDI

Identifiers

Catalog Number
M006840703R0 FDA UDI
Primary DI / UDI-DI
07613353116101 FDA UDI
510(k) Number
K012445 FDA UDI
FDA Product Code
FFK FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4480 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

LithoClast by E.M.S. Electro Medical Systems S.A. — 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 873d0bb0-faf2-4521-82fa-2f3c9d1219d4 36 fields · synced May 30, 2026