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Cryotop®

EUDAMED

Class IIa (EU MDR)

Ref 81229

by Kitazato Corporation

Identity

Device Name
Cryotop® EUDAMED
Model / Reference
81229 EUDAMED

Identifiers

Primary DI / UDI-DI
04573316385919 EUDAMED
Basic UDI-DI
458223146CRYJS EUDAMED
EMDN Code
U08020401 CRYOPRESERVATION CONTAINERS/STRAWS/VIALS FOR ASSISTED REPRODUCTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

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

Cryotop® by Kitazato Corporation — Class IIa — 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
JP-MF-000018374
Authorised Representative
BIOMEDICAL SUPPLY, S.L. ES-AR-000014358

Sources (1)

  • EUDAMED c3ca9182-55f0-454b-9066-f1ce61c4ce0a 61 fields · synced May 23, 2026