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LW Scientific

FDA UDI

Class I (US FDA UDI)

by Lw Scientific, Inc.

Identity

Trade Name
LW Scientific FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
USA MX5 Digital, Swing-out buckets, 8-place 50ml, 5000rpm, 110v FDA UDI
Model / Reference
M5C-BKS8-50T1 FDA UDI
Description
USA MX5 Digital, Swing-out buckets, 8-place 50ml, 5000rpm, 110v FDA UDI

Identifiers

Catalog Number
M5C-BKS8-50T1 FDA UDI
Primary DI / UDI-DI
00664816003718 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
General-purpose centrifuge IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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: General-purpose centrifuge IVD

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

Similar devices

Also classified as General-purpose 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 50f226c2-9c77-4a2d-b61c-d3ce0a7b93f6 34 fields · synced May 29, 2026