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万俏膨体聚四氟乙烯面部植入体

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万俏 is a Other product (Class III device), registered by 上海康宁医疗用品有限公司. Linked registrations: China 国械注准20233131240. Data as of 2026-10-24.

  • Regulatory classOther · Class III device
  • Holder上海康宁医疗用品有限公司
  • JurisdictionsCN
  • Updated2026-10-24 · v1

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

Registration and basics

万俏

Product
Regulatory class
Class III device
Category
Other
China · NMPA device registration
国械注准20233131240
Name on registration
膨体聚四氟乙烯面部植入体
Registrant
上海康宁医疗用品有限公司
First approval
Not obtained from an official source
This certificate issued
2023-08-24
Valid until
2028-08-23
Models and sizes
见附页。
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20233131240 this certificate issued

    Issue date of this certificate, not the first approval

  2. CN

    国械注准20233131240 change

    延续或变更注册获批（受理号 CQD2601109；2026年04月14日医疗器械批准证明文件送达信息）

  3. CN

    国械注准20233131240 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

2
  • 国械注准20233131240: 延续或变更注册获批（受理号 CQD2601109；2026年04月14日医疗器械批准证明文件送达信息）2026-04-13
  • 国械注准20233131240: certificate issued2023-08-24

Sources

1