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常州药物研究所有限公司注射用透明质酸钠溶液

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常州药物研究所有限公司 is a Skin booster product (Class III device), registered by 常州药物研究所有限公司. Linked registrations: China 国械注准20263131179. First approved in China on 2026-06-05 (国械注准20263131179). Data as of 2026-11-02.

  • Regulatory classSkin booster · Class III device
  • Holder常州药物研究所有限公司
  • JurisdictionsCN
  • Updated2026-11-02 · v1

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

Registration and basics

常州药物研究所有限公司

Product
Regulatory class
Class III device
Category
Skin booster
China · NMPA device registration
国械注准20263131179
Name on registration
注射用透明质酸钠溶液
Registrant
常州药物研究所有限公司
First approval
2026-06-05
This certificate issued
2026-06-05
Valid until
2031-06-04
Models and sizes
该产品由预灌封玻璃注射器或西林瓶和封装在注射器或西林瓶中的溶液组成，根据不同容量划分不同规格，包括：0.5mL、1.0mL、1.5mL、2.0mL、2.5mL、3.0mL、4.0mL、5.0mL。
Checked against official page
2026-10-23

Public: fields from the registration record.

Label facts by jurisdiction

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Registration timeline

  1. CN

    国械注准20263131179 first approved

  2. CN

    国械注准20263131179 change

    首次获批（受理号 CQZ2501504；2026年06月08日医疗器械批准证明文件送达信息）

  3. CN

    国械注准20263131179 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
  • 国械注准20263131179: 首次获批（受理号 CQZ2501504；2026年06月08日医疗器械批准证明文件送达信息）2026-06-05

Sources

1