Advanta Slider Gds

FDA UDI

Class II (US FDA UDI)

by Atrium Medical Corp.

Identity

Trade Name: ADVANTA SLIDER GDS FDA UDI
Generic Name: Synthetic vascular graft FDA UDI
Device Name: 5-8MMX45CM, SW, SH, ADVANTA VXT, GDS FDA UDI
Model / Reference: 22116 FDA UDI
Description: 5-8MMX45CM, SW, SH, ADVANTA VXT, GDS FDA UDI

Identifiers

Primary DI / UDI-DI: 00650862221169 FDA UDI
FDA Product Code: DYF FDA UDI
DSY FDA UDI
DWS FDA UDI
GMDN Term: Synthetic vascular graft FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.3450 FDA UDI
870.4500 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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Synthetic vascular graft

Advanta Slider Gds by Atrium Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic vascular graft.

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Gelweave™ — VASCUTEK LTD · Class II
COOK — William Cook Europe ApS · Class III
Gelweave™ — VASCUTEK LTD · Class II
Zenith — WILLIAM A. COOK AUSTRALIA PTY. LTD. · Class III
Gelweave Vascular Prostheses — VASCUTEK LTD · Class II
IMPRA® ePTFE Vascular Grafts — Bard Peripheral Vascular · Class II

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: Atrium Medical Corp.

Sources (1)

FDA UDI c4bca386-3e10-4e1d-8ff9-558f218f74c9 34 fields · synced May 30, 2026