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VasQ

FDA UDI

Class II (US FDA UDI)

by Laminate Medical Technologies Ltd

Identity

Trade Name
VasQ FDA UDI
Generic Name
Arteriovenous fistula extraluminal mesh-sleeve FDA UDI
Device Name
External support for vascular access arteriovenous fistulas FDA UDI
Model / Reference
1 FDA UDI
Description
External support for vascular access arteriovenous fistulas FDA UDI

Identifiers

Catalog Number
FG0031 FDA UDI
Primary DI / UDI-DI
07290016063318 FDA UDI
FDA Product Code
QVQ FDA UDI
GMDN Term
Arteriovenous fistula extraluminal mesh-sleeve FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4600 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Arteriovenous fistula extraluminal mesh-sleeve

VasQ by Laminate Medical Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arteriovenous fistula extraluminal mesh-sleeve.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Laminate Medical Technologies Ltd

Sources (1)

  • FDA UDI eebc9557-819f-40f2-b660-a15a584cf542 34 fields · synced May 30, 2026