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Superfirt

EUDAMED

Class A (EU MDR)

Ref 120mlModel 20ml,30ml, 40ml, 60ml, 80ml,90ml, 100ml, 120ml

by Nanjing Superfit I & E Co., Ltd.

Identity

Trade Name
Superfirt EUDAMED
Device Name
Sample Cup EUDAMED
Model / Reference
20ml,30ml, 40ml, 60ml, 80ml,90ml, 100ml, 120ml EUDAMED
120ml EUDAMED

Identifiers

Primary DI / UDI-DI
06976400132235 EUDAMED
Basic UDI-DI
697640013SAC01DL 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

Superfirt by Nanjing Superfit I & E 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

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Manufacturer

EUDAMED SRN
CN-MF-000040037
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 05a96c9d-2c46-4472-a001-07f598a17f3f 61 fields · synced Jun 18, 2026