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UAW Instrument

FDA UDI

Class U (US FDA UDI)

by Söring GmbH

Identity

Trade Name
UAW Instrument FDA UDI
Generic Name
Soft-tissue ultrasonic surgical system handpiece, reusable FDA UDI
Device Name
UAW instrument, hoof, 60mm, Ø6mm FDA UDI
Model / Reference
97-103 FDA UDI
Description
UAW instrument, hoof, 60mm, Ø6mm FDA UDI

Identifiers

Catalog Number
97-103 FDA UDI
Primary DI / UDI-DI
04250321523535 FDA UDI
510(k) Number
K072904 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Soft-tissue ultrasonic surgical system handpiece, reusable 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Soft-tissue ultrasonic surgical system handpiece, reusable

UAW Instrument by Söring GmbH — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue ultrasonic surgical system handpiece, reusable.

Cleared under the same submission

K072904 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Söring GmbH

Sources (1)

  • FDA UDI 685954b7-faf8-4b69-a95f-e9830abe10a0 36 fields · synced May 31, 2026