← Back to catalogue

Clickline

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
CLICKLINE FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
CLICKLINE Insert Curette, 4,8mm FDA UDI
Model / Reference
28164RS FDA UDI
Description
CLICKLINE Insert Curette, 4,8mm FDA UDI

Identifiers

Primary DI / UDI-DI
04048551106471 FDA UDI
FDA Product Code
GWG FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1480 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery dissector

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

Similar devices

Also classified as Open-surgery dissector.

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 d85e4bad-fce3-42d5-b7c5-4282265401ec 33 fields · synced May 31, 2026