← Back to catalogue

Hemolytic Agent

EUDAMED

Class A (EU MDR)

Ref XQ-0108-01Model HA-1Ref XQ-0108-03

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Hemolytic Agent EUDAMED
Device Name
Hemolytic Agent EUDAMED
Model / Reference
HA-1 EUDAMED
XQ-0108-01 EUDAMED
XQ-0108-03 EUDAMED

Identifiers

Primary DI / UDI-DI
06941377305777 EUDAMED
06941377305791 EUDAMED
Basic UDI-DI
697049309W01030000026A8 EUDAMED
Direct Marketing DI
06941377305777 EUDAMED
06941377305791 EUDAMED
EMDN Code
W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Hemolytic Agent by Shenzhen Dymind Biotechnology 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

EUDAMED SRN
CN-MF-000024842
Authorised Representative
Eunitor GmbH DE-AR-000005081

Sources (2)

  • EUDAMED 82f055fa-579b-4631-a44c-db27bf2704c2 61 fields · synced Jul 30, 2026
  • EUDAMED 3b4e0c47-7aa9-47b6-9b8f-07d5959b4b84 61 fields · synced Jul 30, 2026