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FlowEase [Subcutaneous] Infusion Set, 6mm

EUDAMED

Class IIb (EU MDR)

Ref EU1M3006

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

Identity

Trade Name
FlowEase [Subcutaneous] Infusion Set, 6mm EUDAMED
Device Name
FlowEase EUDAMED
Model / Reference
EU1M3006 EUDAMED

Identifiers

Primary DI / UDI-DI
00850025688499 EUDAMED
Basic UDI-DI
0850025688FlowEaseB7 EUDAMED
EMDN Code
A03040199 INFUSION KITS (WITH OR W/O PUMP), SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

FlowEase [Subcutaneous] Infusion Set, 6mm by Takeda Pharmaceuticals U.S.A., Inc. — Class IIb — 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-MF-000014749
Authorised Representative
Takeda Pharmaceuticals International AG Ireland Branch IE-AR-000037116

Sources (1)

  • EUDAMED ad0c75d6-a6a4-4999-befb-522f6a7154e0 61 fields · synced Jul 11, 2026