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深圳普门科技（国产）聚焦超声皮肤治疗仪

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深圳普门科技（国产） is a Other product (Class III device), registered by /. Linked registrations: China 国械注准20263010880. First approved in China on 2026-04-27 (国械注准20263010880). Data as of 2026-10-24.

  • Regulatory classOther · Class III device
  • Holder/
  • JurisdictionsCN
  • Updated2026-10-24 · v1

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

Registration and basics

深圳普门科技（国产）

Product
Regulatory class
Class III device
Category
Other
China · NMPA device registration
国械注准20263010880
Name on registration
聚焦超声皮肤治疗仪
Registrant
深圳普门科技股份有限公司
First approval
2026-04-27
This certificate issued
2026-04-27
Valid until
2031-04-26
Models and sizes
ProFirm V7、ProFirm V8、ProFirm V9
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20263010880 first approved

  2. CN

    国械注准20263010880 change

    首次获批（受理号 CQZ2500752；2026年04月28日医疗器械批准证明文件送达信息）

  3. CN

    国械注准20263010880 change

    延续或变更注册获批（受理号 CQD2602040；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20263010880 change

    官网变更：载明生产地址由:广东省东莞市松山湖园区彰化路2号1号厂房2-11楼（委托生产）;载明生产地址变更为:1.广东省深圳市龙华区观湖街道观城社区求知东路8号普门科技总部大厦5楼、7-9楼、10楼南、15楼 2.删除备注中“受托生产企业：广东普门生物医疗科技有限公司；统一社会信…

  5. CN

    国械注准20263010880 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20263010880: 延续或变更注册获批（受理号 CQD2602040；2026年07月02日医疗器械批准证明文件送达信息）2026-07-02
  • 国械注准20263010880: 官网变更：载明生产地址由:广东省东莞市松山湖园区彰化路2号1号厂房2-11楼（委托生产）;载明生产地址变更为:1.广东省深圳市龙华区观湖街道观城社区求知东路8号…2026-07-02
  • 国械注准20263010880: 首次获批（受理号 CQZ2500752；2026年04月28日医疗器械批准证明文件送达信息）2026-04-27

Sources

1