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1C63 Trial Foot, L, without Footshell

EUDAMED

Class I (EU MDR)

Ref 1C63=L23-3-P/0-OBModel 1C63

by Otto Bock HealthCare LP

Identity

Trade Name
1C63 Trial Foot, L, without Footshell EUDAMED
Device Name
Triton Low Profile EUDAMED
Model / Reference
1C63 EUDAMED
1C63=L23-3-P/0-OB EUDAMED

Identifiers

Primary DI / UDI-DI
04064409039166 EUDAMED
Basic UDI-DI
406440900000000001C63RW EUDAMED
EMDN Code
Y062409 TRANSTIBIAL PROSTHESES (FOR AMPUTATION UNDER KNEE) 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

1C63 Trial Foot, L, without Footshell by Otto Bock HealthCare LP — 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

EUDAMED SRN
US-MF-000019567
Authorised Representative
Ottobock SE & Co. KGaA DE-AR-000016531

Sources (1)

  • EUDAMED bca8ead4-39cb-4683-92c5-1fa18f83356e 61 fields · synced Sep 17, 2026