Aortic Punch

FDA UDI

Class I (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: Aortic Punch FDA UDI
Generic Name: Aorta punch, single-use FDA UDI
Device Name: Aortic Punch APU430 - 3.0mm punch size FDA UDI
Model / Reference: APU430 FDA UDI
Description: Aortic Punch APU430 - 3.0mm punch size FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000651749 FDA UDI
FDA Product Code: DWS FDA UDI
GMDN Term: Aorta punch, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.4500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Aorta punch, single-use

Aortic Punch by Medtronic, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aorta punch, single-use.

A&E Medical / Rotating Surgical Punches — A & E MEDICAL CORPORATION · Class I
PILLING — TELEFLEX INCORPORATED · Class I
PerfectCut Aortotomy System — QUEST MEDICAL INC · Class I
SCANLAN® Ultimate™ Elliptical Aorta/Vein Punch — SCANLAN INTERNATIONAL INC · Class I
Aorta Punch 14 cm - 5 1/2" Ø 6.0 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
Aorta Punch 14 cm - 5 1/2" Ø 4.0 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I
SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 480d70ab-fc05-42a6-a658-ca86a444658d 36 fields · synced May 30, 2026