Taiwan FDA registration 974b6c2900b3d3ba41e1017a7be7a7d1
"Donghe" Guanjian joint injection (ampoule type)
TW: “東和”關健關節注射劑(安瓿型)
Taiwan·Risk Class 3·TOWA PHARMACEUTICAL CO., LTD., YAMAGATA PLANT·Registered Jan 07, 2011 – Jan 07, 2016CancelledRegistration details
- Analysis ID
- 974b6c2900b3d3ba41e1017a7be7a7d1
- Customs Code
- DHA00602189507
Company information
- Manufacturer
- TOWA PHARMACEUTICAL CO., LTD., YAMAGATA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- STANDARD CHEM. & PHARM. CO., LTD.
Product details
- Intended Use
- IT IS LIMITED TO PATIENTS WITH DEGENERATIVE KNEE ARTHRITIS PAIN WHO DO NOT RESPOND TO CONSERVATIVE NON-PHARMACOLOGICAL TREATMENT AND GENERAL ANALGESICS SUCH AS ACETAMINOPHEN.
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Jan 07, 2011
- Expiry Date
- Jan 07, 2016
- 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 "Donghe" Guanjian joint injection (ampoule type) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 974b6c2900b3d3ba41e1017a7be7a7d1 and manufactured by TOWA PHARMACEUTICAL CO., LTD., YAMAGATA PLANT. The authorized representative in Taiwan is STANDARD CHEM. & PHARM. CO., LTD..
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