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Unidrive

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
UNIDRIVE FDA UDI
Generic Name
Remotely-driven surgical drilling system motor FDA UDI
Device Name
UNIDRIVE® ECO FDA UDI
Model / Reference
20711420 FDA UDI
Description
UNIDRIVE® ECO FDA UDI

Identifiers

Primary DI / UDI-DI
04048551071571 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Remotely-driven surgical drilling system motor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

Category: Remotely-driven surgical drilling system motor

Unidrive by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Remotely-driven surgical drilling system motor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f1aa29b1-87d0-45e2-81c0-60b419ecb2b1 33 fields · synced May 30, 2026