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Visia LungCAD

FDA UDIEUDAMED

Class II (US FDA UDI)

by MeVis Medical Solutions AG

Identity

Trade Name
Visia LungCAD FDA UDI
Generic Name
Radiology DICOM image processing application software FDA UDI
Model / Reference
5.7 FDA UDI

Identifiers

Primary DI / UDI-DI
04260483290015 FDA UDI
FDA Product Code
OEB FDA UDI
GMDN Term
Radiology DICOM image processing application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiology DICOM image processing application software

Visia LungCAD by MeVis Medical Solutions AG — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Radiology DICOM image processing application software.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 41b6bfc2-b3a6-4a24-be4e-b223df6ded48 32 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026