← Back to catalogue

Pack of 10 Drapes for VS3 Iridium Fluorescence (MMS-IR)

FDA UDI

Class II (US FDA UDI)

by Visionsense Ltd.

Identity

Trade Name
Pack of 10 Drapes for VS3 Iridium Fluorescence (MMS-IR) FDA UDI
Generic Name
Endoscope video camera FDA UDI
Model / Reference
VS3-IR FDA UDI

Identifiers

Catalog Number
115-0012 FDA UDI
Primary DI / UDI-DI
18130400103533 FDA UDI
FDA Product Code
JAA FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscope video camera

Pack of 10 Drapes for VS3 Iridium Fluorescence (MMS-IR) by Visionsense Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Visionsense Ltd.

Sources (1)

  • FDA UDI c8a0b2d1-374f-42e6-9988-0de1298de306 33 fields · synced May 30, 2026