Taiwan FDA registration 2500ac20f349b44c9b0198de1303aa59
“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 Oct 29, 2013 – Oct 29, 2018CancelledRegistration details
- Analysis ID
- 2500ac20f349b44c9b0198de1303aa59
- License Form
- Ministry of Health Medical Device Import No. 013540
- Customs Code
- DHA09401354000
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
- Oct 29, 2013
- Expiry Date
- Oct 29, 2018
- 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” 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 2500ac20f349b44c9b0198de1303aa59 and manufactured by PRODUITS DENTAIRES PIERRE ROLLAND SAS (ACTEON GROUP). The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices