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LimFlow Extension Stent Graft

FDA UDI

Class III (US FDA UDI)

by Limflow Inc.

Identity

Trade Name
LimFlow Extension Stent Graft FDA UDI
Generic Name
Arteriovenous endovascular stent-graft FDA UDI
Device Name
LimFlow Extension Stent Graft (5.5 mm x 200 mm). The LimFlow Extension Stent Graft is indicated for patients who have chronic limb-threatening ischemia with no suitable endovascular or surgical revascularization options and are at risk of major amputation. FDA UDI
Model / Reference
RGS-55200-US-24 FDA UDI
Description
LimFlow Extension Stent Graft (5.5 mm x 200 mm). The LimFlow Extension Stent Graft is indicated for patients who have chronic limb-threatening ischemia with no suitable endovascular or surgical revascularization options and are at risk of major amputation. FDA UDI

Identifiers

Primary DI / UDI-DI
00850041730219 FDA UDI
FDA Product Code
QWN FDA UDI
GMDN Term
Arteriovenous endovascular stent-graft 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

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: Arteriovenous endovascular stent-graft

LimFlow Extension Stent Graft by Limflow Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arteriovenous endovascular stent-graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limflow Inc.

Sources (1)

  • FDA UDI e1d227a7-f7cf-49da-9000-921ad864802f 34 fields · synced May 31, 2026