Tps

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: TPS FDA UDI
Generic Name: Foot-switch, electrical FDA UDI
Device Name: Unidirectional Footswitch FDA UDI
Model / Reference: 5100007000 FDA UDI
Description: Unidirectional Footswitch FDA UDI

Identifiers

Catalog Number: 5100007000 FDA UDI
Primary DI / UDI-DI: 04546540401724 FDA UDI
FDA Product Code: EIA FDA UDI
GMDN Term: Foot-switch, electrical FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6640 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Foot-switch, electrical

Tps by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

ElectrodeCRF — Cambridge Interventional LLC · Class IIb
ElectrodeCRF — Cambridge Interventional LLC · Class IIb
Alligature-E — Alan Electronic Systems Private Limited · Class IIb
Sonicure — Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. · U
Arthrex® — Arthrex, Inc. · Class I
CableAME — Cambridge Interventional LLC · Class IIb
PowerPack — MICROLINE SURGICAL, INC. · Class II
Electrosurgical unit Argo Plasma — EMED SP. Z O. O. SP. K. · Class IIb

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI d3f881a8-dee1-439a-bb6c-965acfd50897 36 fields · synced Jun 1, 2026