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Vs3-Mms

FDA UDI

Class I (US FDA UDI)

by Visionsense Ltd.

Identity

Trade Name
VS3-MMS FDA UDI
Generic Name
General-purpose surgical microscope FDA UDI
Device Name
VS3 Pneumatic Arm (SH1) for Miniature Microscope (MMS) FDA UDI
Model / Reference
115-0001 FDA UDI
Description
VS3 Pneumatic Arm (SH1) for Miniature Microscope (MMS) FDA UDI

Identifiers

Catalog Number
115-0001 FDA UDI
Primary DI / UDI-DI
18130400103502 FDA UDI
FDA Product Code
HRM FDA UDI
GMDN Term
General-purpose surgical microscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Vs3-Mms by Visionsense Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Visionsense Ltd.

Sources (1)

  • FDA UDI bdac0c9b-1606-40d2-aef9-7e9c699dea1a 35 fields · synced May 30, 2026