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Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Luer-formatted protective cap FDA UDI
Device Name
CAP,MALE,LUER,LOCK,LIGHT,BLUE,GRIP FDA UDI
Model / Reference
DYNJCAPM2 FDA UDI
Description
CAP,MALE,LUER,LOCK,LIGHT,BLUE,GRIP FDA UDI

Identifiers

Catalog Number
DYNJCAPM2 FDA UDI
Primary DI / UDI-DI
10193489109696 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Luer-formatted protective cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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

Category: Luer-formatted protective cap

Namic by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted protective cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c58059c-468e-4d97-9f77-31789d0e88e6 36 fields · synced Jun 1, 2026