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Night Splint

EUDAMED

Class I (EU MDR)

Ref 620003(S/UNI/Gray&Silver)Model AFO Splint 620001 AFO Leaf Spring 620002 Night Splint:620003 Soft Night Splint:620004 Dorsal Night Splint:620016Ref 620003(L/UNI/Gray&Silver)Ref 620003(M/UNI/Gray&Silver)

by Orthotech Rehabilitation Co., Ltd.

Identity

Trade Name
Night Splint EUDAMED
Device Name
Ankle Brace, Ankle Foot Orthosis, Night Splint (Ankle/foot orthosis) EUDAMED
Model / Reference
AFO Splint 620001 AFO Leaf Spring 620002 Night Splint:620003 Soft Night Splint:620004 Dorsal Night Splint:620016 EUDAMED
620003(S/UNI/Gray&Silver) EUDAMED
620003(L/UNI/Gray&Silver) EUDAMED
620003(M/UNI/Gray&Silver) EUDAMED

Identifiers

Primary DI / UDI-DI
04719964463153 EUDAMED
04719964463177 EUDAMED
04719964463160 EUDAMED
Basic UDI-DI
47199644662WL EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Category: Ankle/foot orthosis

Night Splint by Orthotech Rehabilitation Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000051924
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (3)

  • EUDAMED 78dfe892-a285-4627-aaff-a3b49fb047c3 61 fields · synced Oct 6, 2026
  • EUDAMED 341bca10-e0ec-419a-881a-a13d8861273d 61 fields · synced May 19, 2026
  • EUDAMED 713f7d6c-4697-4b47-9f3e-cb324cd7b074 61 fields · synced May 19, 2026