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Revanesse Contour XLRevanesse Contour XL 10 mL

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Revanesse Contour XL is a Other product (Class III device), registered by Prollenium Medical Technologies Inc.. Linked registrations: EU B-PN40125PY, UK PARD-4165064. Data as of 2026-11-09.

  • Regulatory classOther · Class III device
  • HolderProllenium Medical Technologies Inc.
  • JurisdictionsEU · UK
  • Updated2026-11-09 · v1

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

Registration and basics

Revanesse Contour XL

Product
Regulatory class
Class III device
Category
Other
EU · EUDAMED device record
B-PN40125PY
UK · MHRA device registration (not an approval)
PARD-4165064
Name on registration
Revanesse® Contour XL 10 mL
Registrant
Prollenium Medical Technologies Inc.
EU authorised representative
Emergo Europe B.V.（NL-AR-000000116）
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 B-PN40125PY; 2 registrations linked.This product record is still pending review.

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-4165064 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

1
  • PARD-4165064: registered2023-09-25

Sources

2