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一次性使用治疗头端国械注准20263090749

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一次性使用治疗头端 is a Energy-based device product (Class III device), registered by 威脉清通医疗科技（无锡）有限公司. Linked registrations: China 国械注准20263090749. First approved in China on 2026-04-14 (国械注准20263090749). Data as of 2026-10-24.

  • Regulatory classEnergy-based device · Class III device
  • Holder威脉清通医疗科技（无锡）有限公司
  • JurisdictionsCN
  • Updated2026-10-24 · v1

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

Registration and basics

一次性使用治疗头端

Product
Regulatory class
Class III device
Category
Energy-based device
China · NMPA device registration
国械注准20263090749
Registrant
威脉清通医疗科技（无锡）有限公司
First approval
2026-04-14
This certificate issued
2026-04-14
Valid until
2031-04-13
Models and sizes
YM-TP4-900
Checked against official page
2026-10-23

Public: fields from the registration record.

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Registration timeline

  1. CN

    国械注准20263090749 first approved

  2. CN

    国械注准20263090749 change

    首次获批（受理号 CQZ2501157；2026年04月15日医疗器械批准证明文件送达信息）

  3. CN

    国械注准20263090749 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

1
  • 国械注准20263090749: 首次获批（受理号 CQZ2501157；2026年04月15日医疗器械批准证明文件送达信息）2026-04-14

Sources

1