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Superfirt

EUDAMED

Class A (EU MDR)

Ref 3ulModel 0.1-2.5ul,0.5-10ul,2-20ul,10-100ul,20-200ul, 50-200ul,100-1000ul,1000-5000ul, 5-25ul, 5-50ul,10-50ul, 50-250ul,50-300ul,100-500ul, 200-1000ul,0.4-2ml,1-5ml,2-10ml,5-30ml,10-60ml, 0.1-100ml,10000ul, 2ml,5ml,10ml,25ml,etc

by Nanjing Superfit I & E Co., Ltd.

Identity

Trade Name
Superfirt EUDAMED
Device Name
Pipette EUDAMED
Model / Reference
0.1-2.5ul,0.5-10ul,2-20ul,10-100ul,20-200ul, 50-200ul,100-1000ul,1000-5000ul, 5-25ul, 5-50ul,10-50ul, 50-250ul,50-300ul,100-500ul, 200-1000ul,0.4-2ml,1-5ml,2-10ml,5-30ml,10-60ml, 0.1-100ml,10000ul, 2ml,5ml,10ml,25ml,etc EUDAMED
3ul EUDAMED

Identifiers

Primary DI / UDI-DI
06976400131337 EUDAMED
Basic UDI-DI
697640013PIP01GC EUDAMED
EMDN Code
W050299 DEVICES FOR SAMPLES TRANSPORT - 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

Category: General specimen container IVD, no additive/medium

Superfirt by Nanjing Superfit I & E Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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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 f299fe1c-027a-491a-81d6-f5a3d9e0c444 61 fields · synced Jun 19, 2026