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Cryotubes

EUDAMED

Class A (EU MDR)

Ref TM219-001Model TM219-001,TM219-002,TM219-003,TM219-004,TM219-005,TM219-006, TM219-007,TM219-008,TM219-009,TM219-010,TM219-011,TM219-012, TM219-013,ect

by Ningbo Trustmomed Medical Instruments Company Limited

Identity

Device Name
Cryotubes EUDAMED
Model / Reference
TM219-001,TM219-002,TM219-003,TM219-004,TM219-005,TM219-006, TM219-007,TM219-008,TM219-009,TM219-010,TM219-011,TM219-012, TM219-013,ect EUDAMED
TM219-001 EUDAMED

Identifiers

Primary DI / UDI-DI
06974785212108 EUDAMED
Basic UDI-DI
697478521CRYOTUBESLW EUDAMED
EMDN Code
W0599 IVD GENERAL USE CONSUMABLE DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Cryotubes by Ningbo Trustmomed Medical Instruments Company Limited — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000028659
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED c034ec70-b030-4627-a97a-3452e4eac52e 61 fields · synced Oct 6, 2026