Taiwan FDA registration c0d920acb71902b814dbd9031b53f3d7

"SILVERAID" Endosseous dental implant accessories (Non-Sterile)

TW: "植護芳" 牙齒骨內植入物附件 (未滅菌)

Taiwan·Risk Class 1·MD·SILVERAID S.R.L.·Registered Jan 20, 2021 – Jan 20, 2026Expired

Registration details

Analysis ID: c0d920acb71902b814dbd9031b53f3d7
License Form: Ministry of Health Medical Device Import No. 022263
Customs Code: DHA09402226301

Company information

Manufacturer: SILVERAID S.R.L.
Manufacturer Country: Italy
Authorized Representative: GOETHE BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3980 Dental Intraosseous Implant Attachment
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 20, 2021
Expiry Date: Jan 20, 2026

About this record

Access comprehensive regulatory information for "SILVERAID" Endosseous dental implant accessories (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 c0d920acb71902b814dbd9031b53f3d7 and manufactured by SILVERAID S.R.L.. The authorized representative in Taiwan is GOETHE BIOTECH CO., LTD..

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