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MLL (KMT2A) Breakapart Probe

EUDAMED

Class C (EU MDR)

Ref CE-LPH 013Ref CE-LPH 013-S

by Cytocell Limited

Identity

Trade Name
MLL (KMT2A) Breakapart Probe EUDAMED
Device Name
MLL (KMT2A) Breakapart Probe EUDAMED
Model / Reference
CE-LPH 013 EUDAMED
CE-LPH 013-S EUDAMED

Identifiers

Primary DI / UDI-DI
05055844906242 EUDAMED
05055844923560 EUDAMED
Basic UDI-DI
50558449LPH013J8 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

MLL (KMT2A) Breakapart 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 (2)

  • EUDAMED 41aa1902-426a-4ef3-8c94-6ee592bc729f 61 fields · synced Jul 28, 2026
  • EUDAMED bbaf2b49-fd88-4354-b994-7e95a5969219 61 fields · synced May 17, 2026