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Ellanse MEllanse M Polycaprolactone Microsphere Filler

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Ellanse M is a PCL product (Class III device), registered by 艾克蒂思医疗有限公司AQTIS Medical B.V.. Linked registrations: China 国械注进20263130151. First approved in China on 2026-04-21 (国械注进20263130151). Data as of 2026-10-24.

  • Regulatory classPCL · Class III device
  • Holder艾克蒂思医疗有限公司AQTIS Medical B.V.
  • JurisdictionsCN
  • Updated2026-10-24 · v1

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

Registration and basics

Ellanse M

Product
Regulatory class
Class III device
Category
PCL
China · NMPA device registration
国械注进20263130151
Name on registration
注射用聚己内酯微球面部填充剂Polycaprolactone Gel for Injection
Registrant
艾克蒂思医疗有限公司AQTIS Medical B.V.
China agent
欣可丽美学（杭州）供应链管理有限公司
First approval
2026-04-21
This certificate issued
2026-04-21
Valid until
2031-04-20
Models and sizes
Ellansé-M、1mL/支
Checked against official page
2026-10-23

Public: fields from the registration record.

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Registration timeline

  1. CN

    国械注进20263130151 first approved

  2. CN

    国械注进20263130151 change

    首次获批（受理号 JQZ2500021；2026年04月23日医疗器械批准证明文件送达信息）

  3. CN

    国械注进20263130151 valid until

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.

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Recent changes

1
  • 国械注进20263130151: 首次获批（受理号 JQZ2500021；2026年04月23日医疗器械批准证明文件送达信息）2026-04-21

Sources

1