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GloboTec Junior, in folding box, Size 22

EUDAMED

Class I (EU MDR)

Ref 31080010000022

by Bauerfeind AG

Identity

Trade Name
GloboTec Junior, in folding box, Size 22 EUDAMED
Device Name
GloboTec Junior EUDAMED
Model / Reference
31080010000022 EUDAMED

Identifiers

Primary DI / UDI-DI
04046445911385 EUDAMED
Basic UDI-DI
4046445GTJ00000000UR EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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

Category: Orthotic insole, prefabricated, non-antimicrobial

GloboTec Junior, in folding box, Size 22 by Bauerfeind AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bauerfeind AG
EUDAMED SRN
DE-MF-000007543

Sources (1)

  • EUDAMED bdbce433-3529-4399-b280-ff10a2e80015 61 fields · synced Oct 6, 2026