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Sonopet iQ

FDA UDI

Class U (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Sonopet iQ FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
Wireless FP Receiver for 5500008000 FDA UDI
Model / Reference
5500008300 FDA UDI
Description
Wireless FP Receiver for 5500008000 FDA UDI

Identifiers

Catalog Number
5500-008-300 FDA UDI
Primary DI / UDI-DI
07613327298642 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
U 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Foot-switch, electrical

Sonopet iQ by Stryker Corp. — Class U — 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
Stryker Corp.

Sources (1)

  • FDA UDI 97d3f0c1-e12c-4be2-a7b3-8c42e88df827 36 fields · synced Jun 8, 2026