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Pure Vue

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
Pure Vue FDA UDI
Generic Name
Software upgrade/unlocking key FDA UDI
Device Name
Pure Vue Software expansion FDA UDI
Model / Reference
242329 FDA UDI
Description
Pure Vue Software expansion FDA UDI

Identifiers

Catalog Number
242329 FDA UDI
Primary DI / UDI-DI
10886705032204 FDA UDI
FDA Product Code
FCW FDA UDI
GCJ FDA UDI
GMDN Term
Software upgrade/unlocking key FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Software upgrade/unlocking key

Pure Vue by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Software upgrade/unlocking key.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a1ec76f4-2d28-4c98-beda-285170f7c2df 36 fields · synced Jun 8, 2026