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Sputum Processing Reagent

EUDAMED

Class A (EU MDR)

Ref AS030101Model AutoStreak S1800

by Autobio Diagnostics Co., Ltd.

Identity

Trade Name
Sputum Processing Reagent EUDAMED
Device Name
Sputum Processing Reagent EUDAMED
Model / Reference
AutoStreak S1800 EUDAMED
AS030101 EUDAMED

Identifiers

Primary DI / UDI-DI
06942359531634 EUDAMED
Basic UDI-DI
697015090000170HA EUDAMED
EMDN Code
W0104010899 BUFFERS, STAINS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

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

Sputum Processing Reagent by Autobio Diagnostics 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-000003348
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED d0ccdb8c-9d1d-4c2a-996d-9c4d9bdf1e73 61 fields · synced Jun 18, 2026