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Custom Sensory Suit

EUDAMED

Class I (EU MDR)

Ref DM 39

by DM Orthotics Ltd

Identity

Trade Name
Custom Sensory Suit EUDAMED
Device Name
DMO Custom Sensory Suit EUDAMED
Model / Reference
DM 39 EUDAMED

Identifiers

Primary DI / UDI-DI
05054522002252 EUDAMED
Basic UDI-DI
5054522000139QQ EUDAMED
Direct Marketing DI
05054522002252 EUDAMED
EMDN Code
Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Custom Sensory Suit by DM Orthotics Ltd — Class I — 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

Manufacturer
DM Orthotics Ltd
EUDAMED SRN
GB-MF-000008260
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED 9c4bb3b8-e97d-435b-b8f2-ef2bbd4e38eb 61 fields · synced Aug 4, 2026