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CellaVision® Body Fluid Application DM9600 Non-Expiring License

EUDAMEDFDA UDI

Class A (EU MDR)

Ref CBF-970099

by CellaVision AB

Identity

Trade Name
CellaVision® Body Fluid Application DM9600 Non-Expiring License EUDAMED
CellaVision® Body Fluid Application DM9600 FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
CellaVision® Body Fluid Application EUDAMED
The body fluid application automatically locates and presents cell images on cytocentrifuged body fluid preparations. FDA UDI
Model / Reference
CBF-970099 EUDAMEDFDA UDI
Description
The body fluid application automatically locates and presents cell images on cytocentrifuged body fluid preparations. FDA UDI

Identifiers

Catalog Number
CBF-970099 FDA UDI
Primary DI / UDI-DI
07350040973776 EUDAMEDFDA UDI
Basic UDI-DI
735004097CBFEC EUDAMED
510(k) Number
K102778 FDA UDI
FDA Product Code
JOY FDA UDI
EMDN Code
W02029092 VARIOUS HEMATOLOGY / HISTOLOGY / CYTOLOGY INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE EUDAMED
GMDN Term
Laboratory instrument/analyser application software IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
864.5260 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Sweden 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

CellaVision® Body Fluid Application DM9600 Non-Expiring License by Cellavision AB — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
CellaVision AB
EUDAMED SRN
SE-MF-000002377

Sources (2)

  • EUDAMED 842b56a5-3c2b-4af2-9602-abd5418f607c 61 fields · synced Jun 19, 2026
  • FDA UDI 9f1170d3-4435-4c40-9600-d9bb6fbb9094 36 fields · synced May 30, 2026