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Coleman Luer Lock Cap

FDA UDI

Class II (US FDA UDI)

by Mentor Texas LP

Identity

Trade Name
Coleman Luer Lock Cap FDA UDI
Generic Name
Luer-formatted protective cap FDA UDI
Device Name
Coleman Luer Lock Cap FDA UDI
Model / Reference
COL-LLCAP FDA UDI
Description
Coleman Luer Lock Cap FDA UDI

Identifiers

Catalog Number
COL-LLCAP FDA UDI
Primary DI / UDI-DI
00081317023487 FDA UDI
510(k) Number
K981172 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Luer-formatted protective cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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 protective cap

Coleman Luer Lock Cap by Mentor Texas LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted protective cap.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mentor Texas LP

Sources (1)

  • FDA UDI 99ce393b-b73f-4ad7-afab-f005d962117c 36 fields · synced May 30, 2026