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K6460 Triple Quadrupole MS – AJS

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
K6460 Triple Quadrupole MS – AJS FDA UDI
Generic Name
Liquid chromatography/mass spectrometry (LC/MS) analyser IVD FDA UDI
Device Name
K6460 Triple Quadrupole MS – AJS FDA UDI
Model / Reference
K6460 Triple Quadrupole MS – AJS FDA UDI
Description
K6460 Triple Quadrupole MS – AJS FDA UDI

Identifiers

Primary DI / UDI-DI
05700574007300 FDA UDI
FDA Product Code
DOP FDA UDI
GMDN Term
Liquid chromatography/mass spectrometry (LC/MS) analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2860 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Liquid chromatography/mass spectrometry (LC/MS) analyser IVD

K6460 Triple Quadrupole MS – AJS by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid chromatography/mass spectrometry (LC/MS) analyser IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agilent Technologies Inc.

Sources (1)

  • FDA UDI 0d7a9386-1eb6-4d55-a5a1-350d6dc8db26 35 fields · synced Jun 8, 2026