← Back to catalogue

Superfirt

EUDAMED

Class A (EU MDR)

Ref 20x150mmModel Glass：10*75mm/10*100mm/12*75mm/ 12*120mm/13*75mm/12*100mm/16*100mm/16*150mm/ 16*160/18*180mm/18*110mm/20*150mm/ 25*150mm/ 13*100mm etc. Plastic: 10x50mm/10x60mm/12x60mm/11*55mm/12*75mm/12*100/ 13*75mm/13x100mm/13*150mm/15x100mm/15x150mm /16x100mm/ etc.

by Nanjing Superfit I & E Co., Ltd.

Identity

Trade Name
Superfirt EUDAMED
Device Name
Test Tube EUDAMED
Model / Reference
Glass：10*75mm/10*100mm/12*75mm/ 12*120mm/13*75mm/12*100mm/16*100mm/16*150mm/ 16*160/18*180mm/18*110mm/20*150mm/ 25*150mm/ 13*100mm etc. Plastic: 10x50mm/10x60mm/12x60mm/11*55mm/12*75mm/12*100/ 13*75mm/13x100mm/13*150mm/15x100mm/15x150mm /16x100mm/ etc. EUDAMED
20x150mm EUDAMED

Identifiers

Primary DI / UDI-DI
06976400133812 EUDAMED
Basic UDI-DI
697640013TET01HG 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

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

Manufacturer

Manufacturer
Nanjing Superfit I & E Co., Ltd.
EUDAMED SRN
CN-MF-000040037
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 71fc0024-73b3-4f8d-a460-d9ee92fd2872 61 fields · synced Jun 19, 2026