Taiwan FDA registration 9df75fa7c8313831920499c824aee81d
“Hakomed”Laser therapy device
TW: "賀可美"雷射光療儀
Taiwan·Risk Class 2·MD·HAKOMED ITALIA S.r.l·Registered Aug 21, 2022 – Aug 21, 2027ActiveRegistration details
- Analysis ID
- 9df75fa7c8313831920499c824aee81d
- License Form
- Ministry of Health Medical Device Import No. 035760
- Customs Code
- DHA05603576003
Company information
- Manufacturer
- HAKOMED ITALIA S.r.l
- Manufacturer Country
- Italy
- Authorized Representative
- TOYO ADTEC CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5500 infrared light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 21, 2022
- Expiry Date
- Aug 21, 2027
About this record
Access comprehensive regulatory information for “Hakomed”Laser therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9df75fa7c8313831920499c824aee81d and manufactured by HAKOMED ITALIA S.r.l. The authorized representative in Taiwan is TOYO ADTEC CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices