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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 50 mm x 150 mm, Regular wall FDA UDI
Model / Reference
50P15006 FDA UDI
Description
Impra® ePTFE Cardiovascular Patch 50 mm x 150 mm, Regular wall FDA UDI

Identifiers

Catalog Number
50P15006 FDA UDI
Primary DI / UDI-DI
00801741041518 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
Width — 50 Millimeter FDA UDI
Length — 150 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 00c1ae40-baac-4db9-9faf-40aa038cd9b8 36 fields · synced May 30, 2026