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Dry Incubator / EC10-230MD

EUDAMED

Class IIa (EU MDR)

Ref EC10-230MDModel EC6S-230MR

by ASTEC CO., Ltd

Identity

Trade Name
Dry Incubator / EC10-230MD EUDAMED
Device Name
Dry Incubator EUDAMED
Model / Reference
EC6S-230MR EUDAMED
EC10-230MD EUDAMED

Identifiers

Primary DI / UDI-DI
04580647510118 EUDAMED
Basic UDI-DI
458064751A001IY8 EUDAMED
Direct Marketing DI
04580647510118 EUDAMED
EMDN Code
U080299 DEVICES FOR ASSISTED REPRODUCTION - OTHER EUDAMED

Classification

Device Class
Class IIa 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: Assisted reproduction vitrification carrier

Dry Incubator / EC10-230MD by ASTEC CO., Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction vitrification carrier.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ASTEC CO., Ltd
EUDAMED SRN
JP-MF-000020597
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 7a808ee1-5c39-49d2-a3ba-6969f3f79a30 61 fields · synced Jul 13, 2026