Taiwan FDA registration 5387510312c88ba451d56655fe08b4b7

"ACE" Endosseous Dental Implant Accessories (Non-Sterile)

TW: "亞施" 牙齒骨內植入物附件 (未滅菌)

Taiwan·Risk Class 1·MD·ACE SURGICAL SUPPLY COMPANY, INC.·Registered Nov 11, 2016 – Nov 11, 2026Active

Registration details

Analysis ID: 5387510312c88ba451d56655fe08b4b7
License Form: Ministry of Health Medical Device Import No. 017170
Customs Code: DHA09401717000

Company information

Manufacturer: ACE SURGICAL SUPPLY COMPANY, INC.
Manufacturer Country: United States
Authorized Representative: HUNG KUO MEDICAL INSTRUMENT 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: Nov 11, 2016
Expiry Date: Nov 11, 2026

About this record

Access comprehensive regulatory information for "ACE" 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 5387510312c88ba451d56655fe08b4b7 and manufactured by ACE SURGICAL SUPPLY COMPANY, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..

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