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SonicOne (O.R. & Clinic)

FDA UDI

Class U (US FDA UDI)

by Misonix, LLC

Identity

Trade Name
SonicOne (O.R. & Clinic) FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
SonicOne (O.R. & Clinic) 7/16" Wrench FDA UDI
Model / Reference
E-PWRCH FDA UDI
Description
SonicOne (O.R. & Clinic) 7/16" Wrench FDA UDI

Identifiers

Primary DI / UDI-DI
00841626100923 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Surgical torque wrench, 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

Yes

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: Surgical torque wrench, reusable

SonicOne (O.R. & Clinic) by Misonix, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical torque wrench, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Misonix, LLC

Sources (1)

  • FDA UDI abe3cc03-aa53-4937-af0a-d6235dfc6ec1 33 fields · synced Jun 9, 2026