Taiwan FDA registration 60d763e04012a3f2aa1e0449860f0234
"Zhaohong" medical moist hot compress pack (unsterilized)
TW: “兆鴻”醫療用濕熱敷包（未滅菌）
Taiwan·Risk Class 1·Aimin Eisai Co., Ltd. Plant 2·Registered Mar 08, 2010 – Mar 08, 2015CancelledRegistration details
- Analysis ID
- 60d763e04012a3f2aa1e0449860f0234
Company information
- Manufacturer
- Aimin Eisai Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- INTERMEDIC INC.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Medical Hot and Humid Compress Packs (O.5730)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5730 醫療用濕熱敷包
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Mar 08, 2010
- Expiry Date
- Mar 08, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Zhaohong" medical moist hot compress pack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 60d763e04012a3f2aa1e0449860f0234 and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is INTERMEDIC INC..
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