Taiwan FDA registration 9c0f050624b0f3cb22fa257d5caa60f7
"Donohara" Malay gum needle (unsterilized)
TW: “丼原”馬來膠針（未滅菌）
Taiwan·Risk Class 1·INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.·Registered Dec 05, 2013 – Dec 05, 2018CancelledRegistration details
- Analysis ID
- 9c0f050624b0f3cb22fa257d5caa60f7
Company information
- Manufacturer
- INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3850 Malay gum
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 05, 2013
- Expiry Date
- Dec 05, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Donohara" Malay gum needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c0f050624b0f3cb22fa257d5caa60f7 and manufactured by INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.. The authorized representative in Taiwan is INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD..
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