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ClearGuard™

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
ClearGuard™ FDA UDI
Generic Name
Luer-formatted disinfection cap FDA UDI
Device Name
ClearGuard™ HD 100 Pack FDA UDI
Model / Reference
CGHD-100 FDA UDI
Description
ClearGuard™ HD 100 Pack FDA UDI

Identifiers

Catalog Number
CGHD-100 FDA UDI
Primary DI / UDI-DI
00887709123588 FDA UDI
510(k) Number
K180111 FDA UDI
FDA Product Code
PEH FDA UDI
GMDN Term
Luer-formatted disinfection cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5540 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer-formatted disinfection cap

ClearGuard™ by Icu Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted disinfection cap.

Cleared under the same submission

K180111 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI 13b3ca56-6fbe-4677-a6dc-1e56b47a00fb 36 fields · synced May 30, 2026