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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-12 · Link to EUDAMED

YuranosTM Aortic Extension Stent Graft System

UDI-DI 06938370195658Basic UDI-DI 69383701004900VX

Class III · MDR · Lifetech Scientific (Shenzhen) Co., Ltd.

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No
Certificates

2259149TD13

EU technical documentation assessment · unknown

Notified body: DEKRA Certification B.V. (0344)

Valid from 2026-09-01 · Expiry 2031-08-01

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

2259149CE01

EU quality management system · unknown

Notified body: DEKRA Certification B.V. (0344)

Valid from 2026-08-29 · Expiry 2027-08-01

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Lifetech Scientific (Shenzhen) Co., Ltd.

SRN CN-MF-000001561

CN · Shenzhen

manufacturer

Authorised representative: LifeTech Scientific (Europe) B.V. (NL-AR-000000804)

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/yuranostm-aortic-extension-stent-graft-system-5658 · UDI page: /udi/06938370195658

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