Intergard Synergy Knitted Ultrathin

by Intervascular SAS 15 variants

Ref IGKUT0007-70SG

Active European Union

CE MDR

Valid until

26 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number0384401013833S Basic UDI-DI 00384401013358UDI-DI	Date11 Jun 2026Registered	StatusActive
European Union	CE/MDR	NumberG70 103025 0028	Date27 Mar 2026Issued	StatusActive expires 26 Mar 2031

Certificates

1 certificate · EUDAMED

G70 103025 0028 Active

Technical documentation EU MDR

Certifier

TÜV SÜD Product Service GmbH 0123

Issued
27 Mar 2026

Expires
26 Mar 2031

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Map note: Northern Ireland has no dot of its own.

Specification

EUDAMED

Device Name: Intergard Synergy Antimicrobial Collagen Coated Vascular Grafts
Model / Reference: IGKUT0007-70SG

Primary DI / UDI-DI: 00384401013358
Basic UDI-DI: 0384401013833S
EMDN Code: P070102010101 Dacron vascular prostheses, straight, knitted

Device Class: Class III
EU market of registration: France

Manufacturer details

EUDAMED SRN: FR-MF-000002878

Other devices from Intervascular SAS

Intergard Synergy Knitted Ultrathin

Class III
Intergard Synergy Knitted

Class III
Intergard Knitted

Class III
Hemagard Knitted

Class III
Intergard Woven

Class III
Intergard Synergy Knitted

Class III

See all devices from Intervascular SAS →

Properties

Sterile
Implantable
Animal Tissues
Incorporates Medicinal Product

Other properties (9)

Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No