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强脉冲光治疗仪粤械注准20252090895

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强脉冲光治疗仪 is a Energy-based device product (Class II device), registered by 侨城里（广东）医疗器械有限公司. Linked registrations: China 粤械注准20252090895. Data as of 2026-10-28.

  • Regulatory classEnergy-based device · Class II device
  • Holder侨城里（广东）医疗器械有限公司
  • JurisdictionsCN
  • Updated2026-10-28 · v1

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

Registration and basics

强脉冲光治疗仪

Product
Regulatory class
Class II device
Category
Energy-based device
China · NMPA device registration
粤械注准20252090895
Registrant
侨城里（广东）医疗器械有限公司
First approval
Not obtained from an official source
This certificate issued
2025-06-23
Valid until
2030-06-22
Models and sizes
TCFDA01、TCFDA02、TCFDA12、TCFDA09、TCFDA10、TCFDA11、TCFDA10S、TCFDA06S、TCFDA08S、TCFDA09S
Checked against official page
2026-10-28

Public: fields from the registration record.

Label facts by jurisdiction

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Registration timeline

  1. CN

    粤械注准20252090895 this certificate issued

    Issue date of this certificate, not the first approval

  2. CN

    粤械注准20252090895 change

    : 1、注册人名称由“侨城里（东莞）医疗器械有限公司”变更为“侨城里（广东）医疗器械有限公司”。 2、注册人住所由“广东省东莞市塘厦镇莲湖宝源路6号5号楼302房”变更为“广东省惠州市惠城区水口街道青荔四路30号A1栋7楼705”。 3、生产地址由“广东省东莞市塘厦镇莲湖宝源路6…

  3. CN

    粤械注准20252090895 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
  • 粤械注准20252090895: : 1、注册人名称由“侨城里（东莞）医疗器械有限公司”变更为“侨城里（广东）医疗器械有限公司”。 2、注册人住所由“广东省东莞市塘厦镇莲湖宝源路6号5号楼302…2025-12-02
  • 粤械注准20252090895: certificate issued2025-06-23

Sources

1