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enFuse®

EUDAMED

Class IIb (EU MDR)

Ref 30129930Model On-Body Delivery System

by Enable Injections, Inc.

Identity

Trade Name
enFuse® EUDAMED
Device Name
enFuse® EUDAMED
Model / Reference
On-Body Delivery System EUDAMED
30129930 EUDAMED

Identifiers

Primary DI / UDI-DI
00851869007057 EUDAMED
Basic UDI-DI
0851869007ENFUSECW EUDAMED
EMDN Code
A05010101 ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Category: Elastomeric infusion pump system

enFuse® by Enable Injections — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Elastomeric infusion pump system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000040157
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED a6de6675-1d80-4bec-90f1-204acb9abed6 61 fields · synced Jul 17, 2026