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Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
SYRINGE,12ML,TR/FR,MLL,W/RES,-,PKG FDA UDI
Model / Reference
70087003 FDA UDI
Description
SYRINGE,12ML,TR/FR,MLL,W/RES,-,PKG FDA UDI

Identifiers

Catalog Number
70087003 FDA UDI
Primary DI / UDI-DI
10193489065978 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiographic syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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: Angiographic syringe

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

Similar devices

Also classified as Angiographic syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 280f4174-ac9a-4eee-bd4a-b3dc7641e527 35 fields · synced May 30, 2026