Taiwan FDA registration c3f2ded8bcaa8eda23c3568928d6ecc4

"Zest" endosseous dental implant accessories (Non-Sterile)

TW: "瑟斯特" 牙齒骨內植入物附件 (未滅菌)

Taiwan·Risk Class 1·MD·ZEST ANCHORS, INC.·Registered May 04, 2017 – May 04, 2022Expired

Registration details

Analysis ID: c3f2ded8bcaa8eda23c3568928d6ecc4
License Form: Ministry of Health Medical Device Import No. 017791
Customs Code: DHA09401779106

Company information

Manufacturer: ZEST ANCHORS, INC.
Manufacturer Country: United States
Authorized Representative: JONG SHINN DENTAL ENTERPRISE 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: May 04, 2017
Expiry Date: May 04, 2022

About this record

Access comprehensive regulatory information for "Zest" 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 c3f2ded8bcaa8eda23c3568928d6ecc4 and manufactured by ZEST ANCHORS, INC.. The authorized representative in Taiwan is JONG SHINN DENTAL ENTERPRISE CO., LTD..

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