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Del(20q) Deletion Probe

EUDAMED

Class C (EU MDR)

Ref CE-LPH 020Ref CE-LPH 020-S

by Cytocell Limited

Identity

Trade Name
Del(20q) Deletion Probe EUDAMED
Device Name
Del(20q) Deletion Probe EUDAMED
Model / Reference
CE-LPH 020 EUDAMED
CE-LPH 020-S EUDAMED

Identifiers

Primary DI / UDI-DI
05055844906327 EUDAMED
05055844923577 EUDAMED
05055844906334 EUDAMED
Basic UDI-DI
50558449LPH020J5 EUDAMED
EMDN Code
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED

Classification

Device Class
Class C 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Del(20q) Deletion Probe by Cytocell Limited — Class C — 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

Manufacturer
Cytocell Limited
EUDAMED SRN
GB-MF-000016893
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (3)

  • EUDAMED 9a946a4d-66ea-4122-8273-c65e49495012 61 fields · synced Jul 30, 2026
  • EUDAMED 7cbaa6da-c94b-4579-8770-37c92c602b6a 61 fields · synced Jul 10, 2026
  • EUDAMED ccdc05e1-401f-4a37-badb-f4bedf51cd81 61 fields · synced Jul 30, 2026