← Back to catalogue

Veriti™ Dx 96-Well Thermal Cycler

FDA UDI

Class I (US FDA UDI)

by Life Technologies Holdings Pte. Ltd.

Identity

Trade Name
Veriti™ Dx 96-Well Thermal Cycler FDA UDI
Generic Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Model / Reference
9912 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302000529 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 96-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

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

Manufacturer

Manufacturer
Life Technologies Holdings Pte. Ltd.

Sources (1)

  • FDA UDI b39f6f3f-df39-4f2e-a536-14b61c958f10 32 fields · synced May 30, 2026