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Epic™ Vascular

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Epic™ Vascular FDA UDI
Generic Name
Iliac artery stent, bare-metal FDA UDI
Device Name
Self-Expanding Stent System FDA UDI
Model / Reference
H74939200072070 FDA UDI
Description
Self-Expanding Stent System FDA UDI

Identifiers

Catalog Number
H74939200072070 FDA UDI
Primary DI / UDI-DI
08714729805410 FDA UDI
PMA Number
P110035 FDA UDI
FDA Product Code
NIO FDA UDI
GMDN Term
Iliac artery stent, bare-metal 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

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
MRI Safety
MR Conditional FDA UDI

Category: Iliac artery stent, bare-metal

Epic™ Vascular by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Iliac artery stent, bare-metal.

Cleared under the same submission

P110035 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 2b1770c9-5526-47c7-bd2c-b77601764323 36 fields · synced May 30, 2026