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ABS Impression Tray

EUDAMED

Class I (EU MDR)

Ref 1A5910 #1 Large Upper 12pcs/bag,50bags/ctnModel 1A5940 1A5941 1A5942 1A5943 1A5944 1A5945 1A5801—1A5810 1A5950 —1A5859 1A5980—1A5985 1A5851—1A5860 1A5871—1A5879 1A5831—1A5836 1A5970—1A5977 1A5910—1A5918 1A5988—1A5999

by Shanghai Dochem Industries Co., Ltd.

Identity

Trade Name
ABS Impression Tray EUDAMED
Device Name
Tray EUDAMED
Model / Reference
1A5940 1A5941 1A5942 1A5943 1A5944 1A5945 1A5801—1A5810 1A5950 —1A5859 1A5980—1A5985 1A5851—1A5860 1A5871—1A5879 1A5831—1A5836 1A5970—1A5977 1A5910—1A5918 1A5988—1A5999 EUDAMED
1A5910 #1 Large Upper 12pcs/bag,50bags/ctn EUDAMED

Identifiers

Primary DI / UDI-DI
06977493101245 EUDAMED
Basic UDI-DI
697749310010015V9 EUDAMED
EMDN Code
Q010503 IMPRESSION MATERIAL TRAYS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

ABS Impression Tray by Shanghai Dochem Industries Co., 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

EUDAMED SRN
CN-MF-000014350
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED 1d22b4fb-921c-4f27-aed0-ceaea60704f8-1 61 fields · synced Aug 1, 2026
  • EUDAMED 1d22b4fb-921c-4f27-aed0-ceaea60704f8-2 61 fields · synced Aug 1, 2026