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CTCeptor

EUDAMEDFDA UDI

Class A (EU MDR)

Ref CTM-C2203

by CTCELLS Inc.

Identity

Trade Name
CTCeptor EUDAMEDFDA UDI
Generic Name
Cytological centrifuge IVD FDA UDI
Model / Reference
CTM-C2203 EUDAMED
CTM-C313 FDA UDI

Identifiers

Primary DI / UDI-DI
08800204900005 EUDAMEDFDA UDI
Basic UDI-DI
8800204900005W2 EUDAMED
FDA Product Code
GKH FDA UDI
EMDN Code
W02069004 CYTOCENTRIFUGES EUDAMED
GMDN Term
Cytological centrifuge IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.5240 FDA UDI
Market of Registration
Hungary EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

CTCeptor by CTCELLS, Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CTCELLS Inc.
EUDAMED SRN
KR-MF-000049564
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 33e47530-da68-466e-acbb-8a795598e208 61 fields · synced Jul 18, 2026
  • FDA UDI 2625e91a-530d-422e-b4f3-d40927749a94 32 fields · synced May 29, 2026