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REJURAN iREJURAN

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REJURAN i is a Skin booster product (Class III device), registered by PharmaResearch Co., Ltd.. Linked registrations: EU 0880005100M148257G, UK PARD-5715344, UK PARD-5607356 and 1 more. Data as of 2026-11-09.

  • Regulatory classSkin booster · Class III device
  • HolderPharmaResearch Co., Ltd.
  • JurisdictionsEU · UK · AU
  • Updated2026-11-09 · v1

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

Registration and basics

REJURAN i

Product
Regulatory class
Class III device
Category
Skin booster
EU · EUDAMED device record
0880005100M148257G
UK · MHRA device registration (not an approval)
PARD-5715344
UK · MHRA device registration (not an approval)
PARD-5607356
Australia · TGA ARTG device
412631
Name on registration
REJURAN
Registrant
PharmaResearch Co., Ltd.
EU authorised representative
Obelis s.a.（BE-AR-000000106）
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 0880005100M148257G; 4 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. AU

    412631 ARTG start date

  2. UK

    PARD-5607356 registered

  3. UK

    PARD-5715344 registered

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

2
  • PARD-5715344: registered2026-01-14
  • PARD-5607356: registered2025-10-24

Sources

4