Vari-Lase

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: VARI-LASE FDA UDI
Generic Name: Varicose vein lasing procedure kit FDA UDI
Device Name: Vari-Lase Kit 4F 70cm PT Bright 21G FDA UDI
Model / Reference: IPN913599 FDA UDI
Description: Vari-Lase Kit 4F 70cm PT Bright 21G FDA UDI

Identifiers

Catalog Number: 7173 FDA UDI
Primary DI / UDI-DI: 10841156101015 FDA UDI
FDA Product Code: GEX FDA UDI
GMDN Term: Varicose vein lasing procedure kit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

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

FDA UDI

Dimensions & Sizes

Size: Length — 250 Centimeter FDA UDI
Catheter Gauge — 4 French FDA UDI

Category: Varicose vein lasing procedure kit

Vari-Lase by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 36848bd0-ff3e-4ab9-abcd-a27ae87a40c9 36 fields · synced Jun 6, 2026