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LW Scientific

FDA UDI

Class II (US FDA UDI)

by Lw Scientific, Inc.

Identity

Trade Name
LW Scientific FDA UDI
Generic Name
Microhaematocrit centrifuge IVD FDA UDI
Device Name
MX12 digital centrifuge with 24 place microhematocrit rotor and 12 place microtube rotor .Rpm range 100-12,000rpms 110 volt FDA UDI
Model / Reference
MHC-2412-77T1 FDA UDI
Description
MX12 digital centrifuge with 24 place microhematocrit rotor and 12 place microtube rotor .Rpm range 100-12,000rpms 110 volt FDA UDI

Identifiers

Catalog Number
MHC-2412-77T1 FDA UDI
Primary DI / UDI-DI
00664816003749 FDA UDI
FDA Product Code
GKG FDA UDI
GMDN Term
Microhaematocrit centrifuge IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6400 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microhaematocrit centrifuge IVD

LW Scientific by Lw Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microhaematocrit centrifuge IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lw Scientific, Inc.

Sources (1)

  • FDA UDI d556a571-f3c8-4664-9014-f35276a2d4eb 34 fields · synced May 31, 2026