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Veriti™ Dx 384-Well Thermal Cycler

FDA UDI

Class I (US FDA UDI)

by Life Technologies Holdings Pte. Ltd.

Identity

Trade Name
Veriti™ Dx 384-Well Thermal Cycler FDA UDI
Generic Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Device Name
VERITI DX 384W THERMAL CYCLER FDA UDI
Model / Reference
9913 FDA UDI
Description
VERITI DX 384W THERMAL CYCLER FDA UDI

Identifiers

Primary DI / UDI-DI
10190302000536 FDA UDI
FDA Product Code
OUL FDA UDI
GMDN Term
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thermal cycler nucleic acid amplification analyser IVD, laboratory

Veriti™ Dx 384-Well Thermal Cycler by Life Technologies Holdings Pte. Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermal cycler nucleic acid amplification analyser IVD, laboratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Technologies Holdings Pte. Ltd.

Sources (1)

  • FDA UDI ad078129-a7c9-4407-8ff6-60a95d435289 33 fields · synced May 29, 2026