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Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Contrast medium conservation system FDA UDI
Device Name
CONTRAST CONT.ELONGATED SP ASM PG FDA UDI
Model / Reference
90400839 FDA UDI
Description
CONTRAST CONT.ELONGATED SP ASM PG FDA UDI

Identifiers

Catalog Number
90400839 FDA UDI
Primary DI / UDI-DI
10193489068207 FDA UDI
FDA Product Code
IZI FDA UDI
GMDN Term
Contrast medium conservation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1600 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: Contrast medium conservation system

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

Similar devices

Also classified as Contrast medium conservation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25ee6543-0111-46ff-baca-561e4bd6edda 35 fields · synced Jun 1, 2026