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Xevo

FDA UDIEUDAMED

Class I (US FDA UDI)

by Waters Technologies Corporation

Identity

Trade Name
Xevo FDA UDI
Generic Name
Mass spectrometry analyser IVD FDA UDI
Device Name
Xevo TQ-S, IVD FDA UDI
Model / Reference
186005453IVD FDA UDI
Description
Xevo TQ-S, IVD FDA UDI

Identifiers

Catalog Number
186005453IVD FDA UDI
Primary DI / UDI-DI
00816776020155 FDA UDI
FDA Product Code
DOP FDA UDI
GMDN Term
Mass spectrometry 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: Mass spectrometry analyser IVD

Xevo by Waters Technologies Corporation — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Mass spectrometry analyser IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI a88fc158-73a7-43f4-bba8-9aa737a1e419 35 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026