← Back to catalogue

DataTrak

FDA UDI

Class I (US FDA UDI)

by Thermogenesis Corp.

Identity

Trade Name
DataTrak FDA UDI
Generic Name
Blood centrifugation system containment kit FDA UDI
Device Name
DataTrak Software FDA UDI
Model / Reference
150040 FDA UDI
Description
DataTrak Software FDA UDI

Identifiers

Primary DI / UDI-DI
00886368000841 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Blood centrifugation system containment kit 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood centrifugation system containment kit

DataTrak by Thermogenesis Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood centrifugation system containment kit.

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
Thermogenesis Corp.

Sources (1)

  • FDA UDI 43514390-51f1-4a12-81b4-5b9b735de537 34 fields · synced May 30, 2026