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Impra® ePTFE Cardiovascular Patch

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
Impra® ePTFE Cardiovascular Patch FDA UDI
Generic Name
Cardiovascular patch, synthetic FDA UDI
Device Name
Impra® ePTFE Cardiovascular Patch 30 mm x 30 mm, Regular wall FDA UDI
Model / Reference
30P3006 FDA UDI
Description
Impra® ePTFE Cardiovascular Patch 30 mm x 30 mm, Regular wall FDA UDI

Identifiers

Catalog Number
30P3006 FDA UDI
Primary DI / UDI-DI
00801741041495 FDA UDI
FDA Product Code
DXZ FDA UDI
GMDN Term
Cardiovascular patch, synthetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3470 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI
Width — 30 Millimeter FDA UDI

Category: Cardiovascular patch, synthetic

Impra® ePTFE Cardiovascular Patch by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular patch, synthetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI 7e8ec409-0267-4170-851e-3f8b4d2df60a 36 fields · synced May 30, 2026