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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
Hard-tissue ultrasonic surgical system handpiece tip FDA UDI
Device Name
18cm iQ Micro Claw FDA UDI
Model / Reference
550025B303 FDA UDI
Description
18cm iQ Micro Claw FDA UDI

Identifiers

Catalog Number
5500-25B-303 FDA UDI
Primary DI / UDI-DI
07613327422450 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Hard-tissue ultrasonic surgical system handpiece tip FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Hard-tissue ultrasonic surgical system handpiece tip

Sonopet iQ by Stryker Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hard-tissue ultrasonic surgical system handpiece tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 277eaa84-34fd-4d0c-8221-3159a3aa67d4 36 fields · synced May 31, 2026