← Back to catalogue

Turning Handle

FDA UDI

Class II (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name
Turning Handle FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Accessory for WS-90 FDA UDI
Model / Reference
07052400 FDA UDI
Description
Accessory for WS-90 FDA UDI

Identifiers

Primary DI / UDI-DI
J021070524001 FDA UDI
FDA Product Code
KMW FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Turning Handle by W & H Dentalwerk Bürmoos GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1cbfd04f-a787-4e2b-bbf8-e66d074a7e93 33 fields · synced May 30, 2026