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Adept Medical Antegrade IR Platform

FDA UDI

Class I (US FDA UDI)

by Adept Medical Limited

Identity

Trade Name
Adept Medical Antegrade IR Platform FDA UDI
Generic Name
Instrument table FDA UDI
Device Name
The Antegrade Femoral Access Platform is designed to assist in supporting equipment during the antegrade approach to the femoral artery FDA UDI
Model / Reference
AM0430 FDA UDI
Description
The Antegrade Femoral Access Platform is designed to assist in supporting equipment during the antegrade approach to the femoral artery FDA UDI

Identifiers

Catalog Number
AM0430 FDA UDI
Primary DI / UDI-DI
09421905187275 FDA UDI
FDA Product Code
KMN FDA UDI
GMDN Term
Instrument table FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Liquid Chemical FDA UDI

Category: Instrument table

Adept Medical Antegrade IR Platform by Adept Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument table.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fc4ecb38-e045-4273-8218-e4ab3a780d4b 34 fields · synced May 30, 2026