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景嘉注射用透明质酸钠溶液

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景嘉 is a Skin booster product (Class III device), registered by 浙江景嘉医疗科技有限公司. Linked registrations: China 国械注准20263131236. First approved in China on 2026-06-16 (国械注准20263131236). Data as of 2026-11-02.

  • Regulatory classSkin booster · Class III device
  • Holder浙江景嘉医疗科技有限公司
  • JurisdictionsCN
  • Updated2026-11-02 · v1

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

Registration and basics

景嘉

Product
Regulatory class
Class III device
Category
Skin booster
China · NMPA device registration
国械注准20263131236
Name on registration
注射用透明质酸钠溶液
Registrant
浙江景嘉医疗科技有限公司
First approval
2026-06-16
This certificate issued
2026-06-16
Valid until
2031-06-15
Models and sizes
型号:15mg/mL规格：2.0mL、2.5mL、3.0mL、5.0mL。
Checked against official page
2026-10-23

Public: fields from the registration record.

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. CN

    国械注准20263131236 first approved

  2. CN

    国械注准20263131236 change

    首次获批（受理号 CQZ2500187；2026年06月17日医疗器械批准证明文件送达信息）

  3. CN

    国械注准20263131236 change

    延续或变更注册获批（受理号 CQD2602010；2026年07月02日医疗器械批准证明文件送达信息）

  4. CN

    国械注准20263131236 change

    官网变更：载明生产地址由:浙江省杭州市西湖区三墩镇振中路206 号3 幢三层、二层201 室、一层105 室，2 幢3 楼301 室至318 室。;载明生产地址变更为:浙江省杭州市钱塘区临江街道经五路1288-86号三幢1-2层，五幢3-4层，六幢1层。

  5. CN

    国械注准20263131236 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

3
  • 国械注准20263131236: 延续或变更注册获批（受理号 CQD2602010；2026年07月02日医疗器械批准证明文件送达信息）2026-06-30
  • 国械注准20263131236: 官网变更：载明生产地址由:浙江省杭州市西湖区三墩镇振中路206 号3 幢三层、二层201 室、一层105 室，2 幢3 楼301 室至318 室。;载明生产地址…2026-06-30
  • 国械注准20263131236: 首次获批（受理号 CQZ2500187；2026年06月17日医疗器械批准证明文件送达信息）2026-06-16

Sources

1