Taiwan FDA registration 236acd5c7cfef70db8e8da87511bf92a
“LiteCure” LightForce Deep Tissue Laser Therapy System
TW: “萊特科爾” 雷射系統
Taiwan·Risk Class 2·MD·LITECURE, LLC·Registered Dec 09, 2021 – Dec 09, 2026ActiveRegistration details
- Analysis ID
- 236acd5c7cfef70db8e8da87511bf92a
- License Form
- Ministry of Health Medical Device Import No. 035108
- Customs Code
- DHA05603510803
Company information
- Manufacturer
- LITECURE, LLC
- Manufacturer Country
- United States
- Authorized Representative
- CONTINUOUS INSTRUMENT 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
- Dec 09, 2021
- Expiry Date
- Dec 09, 2026
About this record
Access comprehensive regulatory information for “LiteCure” LightForce Deep Tissue Laser Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 236acd5c7cfef70db8e8da87511bf92a and manufactured by LITECURE, LLC. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT CO., LTD..
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