Taiwan FDA registration 0deb5254eaa848a435134f58eb8c2114
"Zheng Sheng" helium-neon laser accessory (disposable fiber optic needle)
TW: “覲晟”氦氖雷射附件(一次性使用光纖針)
Taiwan·Risk Class 2·NEEDLELESS CORPORATION·Registered Apr 25, 2022 – Apr 25, 2027ActiveRegistration details
- Analysis ID
- 0deb5254eaa848a435134f58eb8c2114
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jin-Cheng Medical Company Limited
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Apr 25, 2022
- Expiry Date
- Apr 25, 2027
About this record
Access comprehensive regulatory information for "Zheng Sheng" helium-neon laser accessory (disposable fiber optic needle) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0deb5254eaa848a435134f58eb8c2114 and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is Jin-Cheng Medical Company Limited.
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