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Neauvia StimulatePARD-3798577

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Neauvia Stimulate is a CaHA product (Class III device), registered by MATEX LAB SpA. Linked registrations: UK PARD-3798577, Australia 458873, Australia 459500. Data as of 2026-11-09.

  • Regulatory classCaHA · Class III device
  • HolderMATEX LAB SpA
  • JurisdictionsUK · AU
  • Updated2026-11-09 · v1

Registration and basics are public; findings and prices need an account

Registration and basics

Neauvia Stimulate

Product
Regulatory class
Class III device
Category
CaHA
UK · MHRA device registration (not an approval)
PARD-3798577
Australia · TGA ARTG device
458873
Australia · TGA ARTG device
459500
Name on registration
NEAUVIA STIMULATE
Registrant
MATEX LAB SPA
UK Responsible Person
Qserve Group UK, Ltd. （UK Responsible Person）
Registered on
2023-03-09
Models and sizes
General Medical Device; Class III
Checked against official page
Not yet checked field by field against the live official page

Public: fields from the registration record.Registrant and dates are from PARD-3798577; 3 registrations linked.

Label facts by jurisdiction

What each jurisdiction's label says for the same attribute; gaps are marked Not reported, irrelevant ones N/A

No data yet

Registration timeline

  1. UK

    PARD-3798577 registered

  2. AU

    458873 ARTG start date

  3. AU

    459500 ARTG start date

First approval, this certificate's issue date (updated after renewals or changes), changes and expiry are listed separately; a missing first approval means it was not obtained from an official source. Up to 6 recent changes per registration; click the number for the full record. Dates on non-Chinese registrations keep the source's wording: UK devices show the registration date (MHRA does not approve them), Australia the ARTG start date, FDA devices the decision date.

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Recent changes

1
  • PARD-3798577: registered2023-03-09

Sources

3