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VivaSight-Max

FDA UDI

Class II (US FDA UDI)

by Etview , Ltd.

Identity

Trade Name
VivaSight-Max FDA UDI
Generic Name
Image display unit, colour FDA UDI
Device Name
Monitor. FDA UDI
Model / Reference
SA00014 FDA UDI
Description
Monitor. FDA UDI

Identifiers

Catalog Number
SA00014 FDA UDI
Primary DI / UDI-DI
07290013745293 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Image display unit, colour FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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: Image display unit, colour

VivaSight-Max by Etview , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Image display unit, colour.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Etview , Ltd.

Sources (1)

  • FDA UDI fd7dc95c-daed-46c9-b500-de4bc31a6be5 35 fields · synced Jun 1, 2026