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IN.PACT™ Admiral™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
IN.PACT™ Admiral™ FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, drug-coated FDA UDI
Device Name
DEB ADM06004008P 06.00 L040 UL0800 US FDA UDI
Model / Reference
ADM06004008P FDA UDI
Description
DEB ADM06004008P 06.00 L040 UL0800 US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169383654 FDA UDI
PMA Number
P140010 FDA UDI
FDA Product Code
ONU FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, drug-coated FDA UDI

Classification

Device Class
Class III 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral angioplasty balloon catheter, drug-coated

IN.PACT™ Admiral™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, drug-coated.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI f45f9e5c-1291-4956-8bca-c3f58cbee777 37 fields · synced May 30, 2026