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Mars

FDA UDI

Class II (US FDA UDI)

by Research Instruments , Ltd.

Identity

Trade Name
MARS FDA UDI
Generic Name
Class-I biological safety cabinet FDA UDI
Device Name
In Vitro Fertilization IVF Workstation FDA UDI
Model / Reference
MARS 900 LAF 3FT MARS WORKSTATION FDA UDI
Description
In Vitro Fertilization IVF Workstation FDA UDI

Identifiers

Catalog Number
WM900 FDA UDI
Primary DI / UDI-DI
00888937024685 FDA UDI
FDA Product Code
PUB FDA UDI
GMDN Term
Class-I biological safety cabinet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6120 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Class-I biological safety cabinet

Mars by Research Instruments , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Class-I biological safety cabinet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Research Instruments , Ltd.

Sources (1)

  • FDA UDI d2077fb3-07aa-4250-9304-8dd1edda9f95 34 fields · synced May 30, 2026