← Back to catalogue

LW Scientific, Inc

FDA UDI

Class I (US FDA UDI)

by Lw Scientific, Inc.

Identity

Trade Name
LW Scientific, Inc FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
Centrifuge; E8 Fixed Speed; 8-place test tube FDA UDI
Model / Reference
E8C-U8AF-1503 FDA UDI
Description
Centrifuge; E8 Fixed Speed; 8-place test tube FDA UDI

Identifiers

Catalog Number
E8C-U8AF-1503 FDA UDI
Primary DI / UDI-DI
00664816000199 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, Inc 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

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

Manufacturer

Manufacturer
Lw Scientific, Inc.

Sources (1)

  • FDA UDI d59c1d4d-f5f8-4db8-aaf7-7cff199f4f0c 34 fields · synced Jun 8, 2026