No Certificate Found

Snapshot 2026-10-12 · Link to EUDAMED

Legacy device

SCANLAN® Lambert‑Kay Aorta Clamp

UDI-DI 00846159008456Basic UDI-DI B-00846159008456

Class I · MDD (legacy) · Scanlan International Inc.

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Identification

Model: —
EMDN: L031306
Issuing agency: GS1
Device status: active
Sterile: No
Implantable: No
Measuring function: No
Reusable surgical: No

Manufacturer

Scanlan International Inc.

SRN US-MF-000010251

US · Saint Paul

manufacturer

Authorised representative: MedEnvoy Global BV (NL-AR-000024028)

Related UDI-DIs

No other UDI-DIs share this Basic UDI-DI in this snapshot.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/scanlan-lambert-kay-aorta-clamp-8456 · UDI page: /udi/00846159008456

All devices from Scanlan International Inc.

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