Taiwan FDA registration 55ad227b7769147e460299dede603202
“Pierre Rolland” Expasyl temporary gingival retraction (non-sterile)
TW: “碧嵐”暫時性排齦膏組 (未滅菌)
Taiwan·Risk Class 1·MD·PRODUITS DENTAIRES PIERRE ROLLAND SAS (ACTEON GROUP)·Registered Apr 01, 2019 – Apr 01, 2024ExpiredRegistration details
- Analysis ID
- 55ad227b7769147e460299dede603202
- License Form
- Ministry of Health Medical Device Import No. 020258
- Customs Code
- DHA09402025801
Company information
- Manufacturer Country
- France
- Authorized Representative
- LA FU INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.
- 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
- Apr 01, 2019
- Expiry Date
- Apr 01, 2024
About this record
Access comprehensive regulatory information for “Pierre Rolland” Expasyl temporary 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 55ad227b7769147e460299dede603202 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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