Taiwan FDA registration 9ec87e9b16a6e0d2a68d2f3ea9c7de9e
“Pierre Rolland” SulcusBlue Gingival retraction (Non-Sterile)
TW: “碧嵐”按壓式排齦膏組(未滅菌)
Taiwan·Risk Class 1·MD·PRODUITS DENTAIRES PIERRE ROLLAND SAS (ACTEON GROUP)·Registered Mar 17, 2014 – Mar 17, 2019CancelledRegistration details
- Analysis ID
- 9ec87e9b16a6e0d2a68d2f3ea9c7de9e
- License Form
- Ministry of Health Medical Device Import No. 013968
- Customs Code
- DHA09401396802
Company information
- Manufacturer Country
- France
- Authorized Representative
- LA FU INDUSTRIAL CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F0001 Gingival drain line
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 17, 2014
- Expiry Date
- Mar 17, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Pierre Rolland” SulcusBlue Gingival retraction (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 9ec87e9b16a6e0d2a68d2f3ea9c7de9e and manufactured by PRODUITS DENTAIRES PIERRE ROLLAND SAS (ACTEON GROUP). The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..
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