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Targetingone

FDA UDI

Class I (US FDA UDI)

by TargetingOne Technology (Beijing) Corporation

Identity

Trade Name
TARGETINGONE FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Device Name
Model: P1, Specification: 64 tests/box. FDA UDI
Model / Reference
Nucleic acid extraction reagent/P1 FDA UDI
Description
Model: P1, Specification: 64 tests/box. FDA UDI

Identifiers

Primary DI / UDI-DI
06974689624175 FDA UDI
FDA Product Code
PEG FDA UDI
GMDN Term
Nucleic acid extraction/isolation kit IVD 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid extraction/isolation kit IVD

Targetingone by TargetingOne Technology (Beijing) Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e54bc6b2-1a85-48f9-904f-ab2f3b026e88 33 fields · synced May 31, 2026