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Sonicfusion

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SONICFUSION FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Handpiece Tip FDA UDI
Model / Reference
1910-1011 FDA UDI
Description
Handpiece Tip FDA UDI

Identifiers

Catalog Number
1910-1011 FDA UDI
Primary DI / UDI-DI
07613327095463 FDA UDI
FDA Product Code
HTY FDA UDI
MAI FDA UDI
GAT FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting 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: Surgical instrument handle, non-torque-limiting

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

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 8541bcf4-b63c-41fa-ad64-1e40cd2da38f 34 fields · synced May 31, 2026