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Clik-FIX

FDA UDI

Class II (US FDA UDI)

by Starboard Medical, Inc.

Identity

Trade Name
Clik-FIX FDA UDI
Generic Name
Peripheral intravenous catheterization support kit FDA UDI
Device Name
IV Start Kit with Clik-FIX Universal Hub Securement FDA UDI
Model / Reference
LLSK-1024 FDA UDI
Description
IV Start Kit with Clik-FIX Universal Hub Securement FDA UDI

Identifiers

Catalog Number
LLSK-1024 FDA UDI
Primary DI / UDI-DI
10850933007204 FDA UDI
FDA Product Code
LRS FDA UDI
GMDN Term
Peripheral intravenous catheterization support kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Peripheral intravenous catheterization support kit

Clik-FIX by Starboard Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous catheterization support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Starboard Medical, Inc.

Sources (1)

  • FDA UDI 5bd07e4a-9f01-4428-b099-3541d256e314 34 fields · synced May 30, 2026