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Superfirt

EUDAMED

Class A (EU MDR)

Ref 10mlModel 0.5ml/1ml/1.5ml/1.8ml/2ml/5ml/10ml

by Nanjing Superfit I & E Co., Ltd.

Identity

Trade Name
Superfirt EUDAMED
Device Name
Cryo Tube EUDAMED
Model / Reference
0.5ml/1ml/1.5ml/1.8ml/2ml/5ml/10ml EUDAMED
10ml EUDAMED

Identifiers

Primary DI / UDI-DI
06976400130798 EUDAMED
Basic UDI-DI
697640013CRT01EG 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 4aee3fa0-f9cb-41b3-a7fe-8bf5ab402082 61 fields · synced Jun 19, 2026