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Administration pack for Veyvondi

EUDAMED

Class IIa (EU MDR)

Ref 5500359

by Takeda Pharmaceuticals U.S.A., Inc.

Identity

Trade Name
Administration pack for Veyvondi EUDAMED
Device Name
Administration Pack for Veyvondi EUDAMED
Model / Reference
5500359 EUDAMED

Identifiers

Primary DI / UDI-DI
00850025688277 EUDAMED
Basic UDI-DI
0850025688Veyvondi_PackFK EUDAMED
EMDN Code
A030499 ADMINISTRATION KITS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Medical Purpose
The Administration Pack is intended for administration of reconstituted VEYVONDI by health care professionals or patient self-administration as indicated by their treating physician and described in the product leaflet of VEYVONDI. EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Administration pack for Veyvondi by Takeda Pharmaceuticals U.S.A., Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-PR-000007896

Sources (1)

  • EUDAMED b9382560-c017-4d58-b83f-53e59465630a 61 fields · synced Jun 20, 2026