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BioMimics 3D Vascular Stent System

FDA UDI

Class III (US FDA UDI)

by Veryan Medical, Ltd.

Identity

Trade Name
BioMimics 3D Vascular Stent System FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
BioMimics 3D Vascular Stent System 5.0 x 100 mm FDA UDI
Model / Reference
142122-09 FDA UDI
Description
BioMimics 3D Vascular Stent System 5.0 x 100 mm FDA UDI

Identifiers

Catalog Number
142122-09 FDA UDI
Primary DI / UDI-DI
05391526850442 FDA UDI
PMA Number
P180003 FDA UDI
FDA Product Code
NIP FDA UDI
GMDN Term
Peripheral artery stent, bare-metal FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Stent Diameter — 5.0 Millimeter FDA UDI
Stent Length — 100 Millimeter FDA UDI
Shaft Length — 113 Centimeter FDA UDI

BioMimics 3D Vascular Stent System by Veryan Medical, Ltd. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P180003 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Veryan Medical, Ltd.

Sources (1)

  • FDA UDI 4425cf47-b7ba-4097-adb6-864e6686a5e3 39 fields · synced Jun 1, 2026