Taiwan FDA registration be43c733664204e654775ea8c5d2816a
"Hranik" Numida infrared system
TW: “赫拉尼克”紐邁達紅外線系統
Taiwan·Risk Class 2·HIRONIC CO., LTD.·Registered Oct 17, 2011 – Oct 17, 2016CancelledRegistration details
- Analysis ID
- be43c733664204e654775ea8c5d2816a
- Customs Code
- DHA00602284306
Company information
- Manufacturer
- HIRONIC CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Haotian Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5500 Infrared lamp
- Import Information
- import
Dates and status
- Registration Date
- Oct 17, 2011
- Expiry Date
- Oct 17, 2016
- Cancellation Date
- Feb 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 註銷藥商許可執照
About this record
Access comprehensive regulatory information for "Hranik" Numida infrared system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be43c733664204e654775ea8c5d2816a and manufactured by HIRONIC CO., LTD.. The authorized representative in Taiwan is Haotian Biotechnology 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