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CellaVision DC-1 PPA

FDA UDI

Class II (US FDA UDI)

by Cellavision AB

Identity

Trade Name
CellaVision DC-1 PPA FDA UDI
Generic Name
Cell morphology analyser IVD, automated/semi-automated FDA UDI
Model / Reference
XU-10302 FDA UDI

Identifiers

Primary DI / UDI-DI
07350040975107 FDA UDI
510(k) Number
K200595 FDA UDI
FDA Product Code
JOY FDA UDI
GMDN Term
Cell morphology analyser IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cell morphology analyser IVD, automated/semi-automated

CellaVision DC-1 PPA by Cellavision AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cell morphology analyser IVD, automated/semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cellavision AB

Sources (1)

  • FDA UDI 1437274f-d8b4-4d2e-9bab-e2b7f6e20940 33 fields · synced Jun 8, 2026