Taiwan FDA registration b9a61dec6257d0c11cf8bb6418923783
“HOMETECH” Hot/Cold pack(Non-Sterile)
TW: “虹泰” 冷熱敷包(未滅菌)
Registration details
- Analysis ID
- b9a61dec6257d0c11cf8bb6418923783
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000640
- Customs Code
- DHY08300064009
Company information
- Manufacturer
- Hongtai Enterprise Co., Ltd. Rende Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HOME CARE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Medical equipment that provides hot or cold compresses on the body surface.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5700 Medical Cold Pack
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “HOMETECH” Hot/Cold pack(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b9a61dec6257d0c11cf8bb6418923783 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is HOME CARE TECHNOLOGY 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