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Resin

EUDAMED

Class I (EU MDR)

Ref Model RX

by Shanghai Maxflex Medical Technology Co., Ltd.

Identity

Trade Name
Resin EUDAMED
Device Name
Resin EUDAMED
Model / Reference
Model RX EUDAMED

Identifiers

Primary DI / UDI-DI
06975063094515 EUDAMED
Basic UDI-DI
697506309RX3P EUDAMED
Direct Marketing DI
06975063094515 EUDAMED
EMDN Code
Q0102050101 TEMPORARY TEETH RESINS 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: Dental appliance fabrication material, resin

Resin by Shanghai Maxflex Medical Technology Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000032435
Authorised Representative
Everbiz GmbH DE-AR-000008964

Sources (1)

  • EUDAMED 4b608c3b-6d93-4b06-9801-181e4101f530 61 fields · synced Jun 17, 2026