← Back to catalogue

Base Mold

EUDAMED

Class A (EU MDR)

Ref MO01-0707Model MO01-0707,MO01-1515 ,MO01-2424,MO01-2430,MO01-2437 ,MO02-0707,MO02-1515,MO02-2424,MO02-2430,MO02-2437

by Nantong Mevid Life Scientific Co., Ltd

Identity

Device Name
Base Mold EUDAMED
Model / Reference
MO01-0707,MO01-1515 ,MO01-2424,MO01-2430,MO01-2437 ,MO02-0707,MO02-1515,MO02-2424,MO02-2430,MO02-2437 EUDAMED
MO01-0707 EUDAMED

Identifiers

Primary DI / UDI-DI
06976529296009 EUDAMED
Basic UDI-DI
697652929BM01P2 EUDAMED
EMDN Code
W0202059004 TISSUE EMBEDDING PROCESSORS 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Base Mold by Nantong Mevid Life Scientific Co., Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000036513
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED 1993bd3d-1623-42c1-a2f6-8ca086c1e114 61 fields · synced Jul 29, 2026