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Remote Review Software Version Independent

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AG516335

by CellaVision AB

Identity

Trade Name
Remote Review Software Version Independent EUDAMED
DI Remote Review Software version 6.x.x FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
CellaVision® Review Software EUDAMED
The CellaVision remote review software enable remote users to access data collected, stored and processed by DI-60 with the ability to reclassify cells and sign off slides from another location. FDA UDI
Model / Reference
AG516335 EUDAMEDFDA UDI
Description
The CellaVision remote review software enable remote users to access data collected, stored and processed by DI-60 with the ability to reclassify cells and sign off slides from another location. FDA UDI

Identifiers

Catalog Number
AG516335 FDA UDI
Primary DI / UDI-DI
07350040975930 EUDAMEDFDA UDI
Basic UDI-DI
735004097CRRSB5 EUDAMED
510(k) Number
K092868 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

Remote Review Software Version Independent by Cellavision AB — 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

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

Manufacturer

Manufacturer
CellaVision AB
EUDAMED SRN
SE-MF-000002377

Sources (2)

  • EUDAMED a0ae8c27-3c07-45dd-9f9c-601f06d2e0bb 61 fields · synced Jun 18, 2026
  • FDA UDI d41f6ca8-7d29-448e-acc0-ab94c749d4b9 36 fields · synced May 30, 2026