← Back to catalogue

Take-Apart

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 26167FGR

by Karl Storz GmbH & Co. KG

Identity

Trade Name
TAKE-APART FDA UDI
Generic Name
Electrosurgical handpiece, reusable FDA UDI
Device Name
Handles, dismountable instruments EUDAMED
handle FDA UDI
Model / Reference
26167FGR EUDAMEDFDA UDI
Description
handle FDA UDI

Identifiers

Catalog Number
26167FGR FDA UDI
Primary DI / UDI-DI
04048551095324 EUDAMEDFDA UDI
Basic UDI-DI
4048551000787UM EUDAMED
FDA Product Code
GCJ FDA UDI
EMDN Code
Z12010980 ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrosurgical handpiece, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical handpiece, reusable

Take-Apart by Karl Storz GmbH & Co. KG — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 4c79952e-ab31-4d29-9714-6091d4e4335b 35 fields · synced Jul 24, 2026
  • EUDAMED 76f45ba9-78ba-4311-ab11-fc0050e48960 61 fields · synced Jul 24, 2026