Tack Endovascular System (6F, 4.0-8.0mm)

FDA UDI

Class III (US FDA UDI)

by Intact Vascular, Inc.

Identity

Trade Name: Tack Endovascular System (6F, 4.0-8.0mm) FDA UDI
Generic Name: Peripheral artery stent, bare-metal FDA UDI
Device Name: 135cm Catheter Length FDA UDI
Model / Reference: 206135061 FDA UDI
Description: 135cm Catheter Length FDA UDI

Identifiers

Catalog Number: 206135061 FDA UDI
Primary DI / UDI-DI: 00850003494036 FDA UDI
FDA Product Code: QCT FDA UDI
GMDN Term: Peripheral 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

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Catheter Length — 135 Centimeter FDA UDI

Category: Peripheral artery stent, bare-metal

Tack Endovascular System (6F, 4.0-8.0mm) by Intact Vascular, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral artery stent, bare-metal.

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Absolute Pro — Abbott Vascular · Class III
Protégé™ GPS™ — EV3, INC · Class II
COMPLETE® SE VASCULAR — MEDTRONIC, INC. · Class III
Zilver 518 — Cook Ireland, Ltd. · Class III

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Intact Vascular, Inc.

Sources (1)

FDA UDI 9270fba3-2786-4ddd-bd1e-26300da91146 37 fields · synced May 30, 2026