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Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Angiography kit FDA UDI
Device Name
MTO-LHK-FHN MEMORIAL HOSPITAL FDA UDI
Model / Reference
63060921 FDA UDI
Description
MTO-LHK-FHN MEMORIAL HOSPITAL FDA UDI

Identifiers

Catalog Number
63060921 FDA UDI
Primary DI / UDI-DI
10193489058024 FDA UDI
FDA Product Code
OEZ FDA UDI
GMDN Term
Angiography kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

Yes

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: Angiography kit

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

Similar devices

Also classified as Angiography kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4006aa25-d0e7-4f91-ac4f-6ac46a15fb5b 35 fields · synced May 30, 2026