← Back to catalogue

Clickline

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 26310

by Karl Storz GmbH & Co. KG

Identity

Trade Name
CLICKLINE FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Instrument handles, gynecology EUDAMED
CLICKLINE Metal Handle, without ratchet FDA UDI
Model / Reference
26310 EUDAMEDFDA UDI
Description
CLICKLINE Metal Handle, without ratchet FDA UDI

Identifiers

Catalog Number
26310 FDA UDI
Primary DI / UDI-DI
04048551426852 EUDAMEDFDA UDI
Basic UDI-DI
4048551000697UK EUDAMED
FDA Product Code
NWW FDA UDI
EMDN Code
Z12080280 GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
884.1690 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

Yes

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

Clickline by Karl Storz GmbH & Co. KG — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

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 d41e43ac-f7a5-4c4e-91ad-2610310b596f 35 fields · synced Jun 18, 2026
  • EUDAMED 244eecbf-8159-44ac-a5a4-ae8f86d2c782 61 fields · synced Jun 18, 2026