Taiwan FDA registration b85e57cacf3e27a54fcba92bf974a4bf
"TEN" COLD PACK(Non-Sterile)
TW: "朝揚" 冷敷袋(未滅菌)
Registration details
- Analysis ID
- b85e57cacf3e27a54fcba92bf974a4bf
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000365
- Customs Code
- DHY08300036500
Company information
- Manufacturer
- Chaoyang Plastic Factory Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Chaoyang Plastic Factory Co., Ltd
Product details
- Intended Use
- Provide cold compress treatment 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, 2025
About this record
Access comprehensive regulatory information for "TEN" 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 b85e57cacf3e27a54fcba92bf974a4bf and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory 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