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Infiniti™ Ambi

FDA UDI

Class II (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name
INFINITI™ AMBI FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
5F INFINITI AMBI 125CM TG 4.0 FDA UDI
Model / Reference
555525T401 FDA UDI
Description
5F INFINITI AMBI 125CM TG 4.0 FDA UDI

Identifiers

Catalog Number
555525T401 FDA UDI
Primary DI / UDI-DI
10705032100113 FDA UDI
510(k) Number
K232573 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use 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

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 catheter, single-use

Infiniti™ Ambi by Cordis US Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis US Corp.

Sources (1)

  • FDA UDI 20148c6c-ffec-4a6b-a99a-3a4585e28d31 35 fields · synced May 30, 2026