Identity

Trade Name
NAMIC FDA UDI
Generic Name
Angiography kit FDA UDI
Device Name
NAMIC Convenience Kit FDA UDI
Model / Reference
65120098 FDA UDI
Description
NAMIC Convenience Kit FDA UDI

Identifiers

Primary DI / UDI-DI
H965651200980 FDA UDI
GMDN Term
Angiography kit FDA UDI

Classification

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

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: Angiography kit

Namic by Navilyst Medical, Inc. — 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 761b7792-0d53-4e25-b2b3-3d1b4f14be91 34 fields · synced Jun 1, 2026