← Back to catalogue

Graft Sizer Set

FDA UDI

Class II (US FDA UDI)

by Vascutek Ltd

Identity

Trade Name
Graft Sizer Set FDA UDI
Generic Name
Open-surgery blood vessel sizer, single-use FDA UDI
Device Name
Graft Sizer Set FDA UDI
Model / Reference
GSS002 FDA UDI
Description
Graft Sizer Set FDA UDI

Identifiers

Catalog Number
GSS002 FDA UDI
Primary DI / UDI-DI
05037881038919 FDA UDI
FDA Product Code
DSY FDA UDI
GMDN Term
Open-surgery blood vessel sizer, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3450 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Graft Sizer Set by Vascutek Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Vascutek Ltd

Sources (1)

  • FDA UDI 14542861-a699-4706-b49a-f17e408a2b5e 38 fields · synced May 30, 2026