← Back to catalogue

Paradigm ClickLok

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
Paradigm ClickLok FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
Paradigm ClickLok Drill Bit, 2.1 mm FDA UDI
Model / Reference
PASDB FDA UDI
Description
Paradigm ClickLok Drill Bit, 2.1 mm FDA UDI

Identifiers

Catalog Number
PASDB FDA UDI
Primary DI / UDI-DI
20653405986789 FDA UDI
FDA Product Code
GFG FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Fluted surgical drill bit, single-use

Paradigm ClickLok by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

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

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 0c1ad628-a5ea-4b01-8e20-b60f1ded2e66 36 fields · synced May 30, 2026