Taiwan FDA registration 2999ecc43f8ae984164e5af0f181e442
“LaMeditech” Handy Ray
TW: “拉美迪克”採血器
Taiwan·Risk Class 2·MD·LaMeditech Co., Ltd·Registered Apr 10, 2019 – Apr 10, 2024ExpiredRegistration details
- Analysis ID
- 2999ecc43f8ae984164e5af0f181e442
- License Form
- Ministry of Health Medical Device Import No. 032502
- Customs Code
- DHA05603250205
Company information
- Manufacturer
- LaMeditech Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 10, 2019
- Expiry Date
- Apr 10, 2024
About this record
Access comprehensive regulatory information for “LaMeditech” Handy Ray in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2999ecc43f8ae984164e5af0f181e442 and manufactured by LaMeditech Co., Ltd. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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