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Sputum Processing Reagent

EUDAMED

Class A (EU MDR)

Ref AS030103Model AutoStreak S1800Ref AS030102

by Autobio Diagnostics Co., Ltd.

Identity

Trade Name
Sputum Processing Reagent EUDAMED
Device Name
Sputum Processing Reagent EUDAMED
Model / Reference
AutoStreak S1800 EUDAMED
AS030103 EUDAMED
AS030102 EUDAMED

Identifiers

Primary DI / UDI-DI
06942359531658 EUDAMED
06942359531641 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 (2)

  • EUDAMED a1e8184c-c2a3-473a-8524-ce7d5500b88d 61 fields · synced Aug 1, 2026
  • EUDAMED 186776e2-5665-4db9-ab37-22f293982086 61 fields · synced May 11, 2026