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注射用交联透明质酸钠凝胶注射用交联透明质酸钠凝胶조직수복용생체재료

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注射用交联透明质酸钠凝胶 is a Hyaluronic acid filler product (Class III device), registered by Dong Bang Medical Co.,Ltd.. Linked registrations: China 国械注进20223130127. Data as of 2026-10-24.

  • Regulatory classHyaluronic acid filler · Class III device
  • HolderDong Bang Medical Co.,Ltd.
  • JurisdictionsCN
  • Updated2026-10-24 · v1

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

Registration and basics

注射用交联透明质酸钠凝胶

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
China · NMPA device registration
国械注进20223130127
Name on registration
注射用交联透明质酸钠凝胶조직수복용생체재료
Registrant
株式会社东方医疗 Dong Bang Medical Co.,Ltd.
China agent
东邦生物科技（北京）有限公司
First approval
Not obtained from an official source
This certificate issued
2022-03-02
Valid until
2027-03-01
Models and sizes
D24P、D24C
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

AttributeChina label
Storage规格型号 D24P：避光

Each cell is extracted from that jurisdiction's label; click the number for the original passage. “—” means nothing has been extracted for it yet, not that the label is silent. 1 of them are not yet reviewed by a person.

Registration timeline

  1. CN

    国械注进20223130127 this certificate issued

    Issue date of this certificate, not the first approval

  2. CN

    国械注进20223130127 change

    官网变更：一 、产品型号由D24P变更为D24P、D24C。二、产品结构组成由“该产品由预罐封玻璃注射器、不锈钢注射针和封装在注射器中的凝胶颗粒悬液组成。凝胶颗粒悬液由经交联的透明质酸钠、氯化钠、磷酸二氢钾、磷酸氢钠十二水合物及注射用水组成，其中透明质酸钠由微生物发酵法制备，标示…

  3. CN

    国械注进20223130127 change

    一 、产品型号由D24P变更为D24P、D24C。二、产品结构组成由“该产品由预罐封玻璃注射器、不锈钢注射针和封装在注射器中的凝胶颗粒悬液组成。凝胶颗粒悬液由经交联的透明质酸钠、氯化钠、磷酸二氢钾、磷酸氢钠十二水合物及注射用水组成，其中透明质酸钠由微生物发酵法制备，标示浓度为 2…

  4. CN

    国械注进20223130127 change

    延续或变更注册获批（受理号 JQX2501145；2026年03月20日医疗器械批准证明文件送达信息）

  5. CN

    国械注进20223130127 change

    官网变更：产品技术要求变更详见产品技术要求变更对比表。

  6. CN

    国械注进20223130127 change

    产品技术要求变更详见产品技术要求变更对比表。

  7. CN

    国械注进20223130127 change

    延续或变更注册获批（受理号 JQY2600467；2026年07月03日医疗器械批准证明文件送达信息）

  8. CN

    国械注进20223130127 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

5
  • 国械注进20223130127: 延续或变更注册获批（受理号 JQY2600467；2026年07月03日医疗器械批准证明文件送达信息）2026-07-02
  • 国械注进20223130127: 延续或变更注册获批（受理号 JQX2501145；2026年03月20日医疗器械批准证明文件送达信息）2026-03-18
  • 国械注进20223130127: 官网变更：产品技术要求变更详见产品技术要求变更对比表。2026-03-18
  • 国械注进20223130127: 产品技术要求变更详见产品技术要求变更对比表。2026-03-18
  • 国械注进20223130127: 一 、产品型号由D24P变更为D24P、D24C。二、产品结构组成由“该产品由预罐封玻璃注射器、不锈钢注射针和封装在注射器中的凝胶颗粒悬液组成。凝胶颗粒悬液由经…2025-04-07

Sources

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