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EZ Single Cytofunnel™, White

EUDAMEDFDA UDI

Class A (EU MDR)

Ref A78710003

by Shandon Diagnostics Limited

Identity

Trade Name
EZ Single Cytofunnel™, White EUDAMED
Epredia FDA UDI
Generic Name
Cytological centrifuge IVD FDA UDI
Device Name
Cytospin 4 Cytocentrifuge EUDAMED
Cytospin 4 Cytocentrifuge - Accessory FDA UDI
Model / Reference
A78710003 EUDAMED
EZ Cytofunnel Single FDA UDI
Description
Cytospin 4 Cytocentrifuge - Accessory FDA UDI

Identifiers

Catalog Number
A78710003 FDA UDI
Primary DI / UDI-DI
05051663625272 EUDAMEDFDA UDI
Basic UDI-DI
5051663SDL012K7 EUDAMED
Unit of Use DI
05051663000192 EUDAMED
FDA Product Code
IFB FDA UDI
EMDN Code
W02069003 CENTRIFUGES EUDAMED
GMDN Term
Cytological centrifuge IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.3300 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose centrifuge IVD

EZ Single Cytofunnel™, White by Shandon Diagnostics Limited — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000008187
Authorised Representative
Epredia Netherlands B.V. NL-AR-000001488

Sources (2)

  • EUDAMED 2686a96e-0f0d-4d96-865b-ecdf42c8ce2b 61 fields · synced Jun 19, 2026
  • FDA UDI 9ea5f4c4-c834-4ee3-b8e3-ee040b73364a 34 fields · synced May 30, 2026