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Aliaxin is a Hyaluronic acid filler product (Class III device), registered by Rose Pharma SA. Linked registrations: EU 764018792ANCLHAER, EU 764018792IDCLHAEK, EU B-07640187920604 and 5 more. Data as of 2026-11-09.

  • Regulatory classHyaluronic acid filler · Class III device
  • HolderRose Pharma SA
  • JurisdictionsEU · UK · AU
  • Updated2026-11-09 · v1

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

Registration and basics

Aliaxin

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
EU · EUDAMED device record
764018792ANCLHAER
EU · EUDAMED device record
764018792IDCLHAEK
EU · EUDAMED device record
B-07640187920604
EU · EUDAMED device record
B-07640187920611
EU · EUDAMED device record
B-07640187920628
EU · EUDAMED device record
B-07640187920635
EU · EUDAMED device record
B-07640187920642
EU · EUDAMED device record
B-07640187920659
Other registrations
21 more, see the timeline
Name on registration
ALIAXIN/NUAVIS
Registrant
Rose Pharma S.A.
First approval
Not obtained from an official source
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 764018792ANCLHAER; 29 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

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Registration timeline

  1. UK

    PARD-572243 registered

  2. AU

    484550 ARTG start date

  3. AU

    484552 ARTG start date

  4. AU

    485546 ARTG start date

  5. AU

    486345 ARTG start date

  6. AU

    486346 ARTG start date

  7. AU

    486347 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-572243: registered2021-03-23

Sources

15