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Sonicfusion

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SONICFUSION FDA UDI
Generic Name
Ultrasonic surgical system torque wrench, reusable FDA UDI
Device Name
TipTool FDA UDI
Model / Reference
1910-1020 FDA UDI
Description
TipTool FDA UDI

Identifiers

Catalog Number
1910-1020 FDA UDI
Primary DI / UDI-DI
07613327096033 FDA UDI
FDA Product Code
HTY FDA UDI
MAI FDA UDI
GAT FDA UDI
GMDN Term
Ultrasonic surgical system torque wrench, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
878.5000 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ultrasonic surgical system torque wrench, reusable

Sonicfusion by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic surgical system torque wrench, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI baa7871e-7f49-4383-942b-392ccd6c9d77 34 fields · synced May 30, 2026