Taiwan FDA registration 4fbd8c13c8dab9a0e00c9bbccd2f5d7b

"I DO" Endosseous dental implant accessories (Non-Sterile)

TW: "艾德" 牙齒骨內植入物附件 (未滅菌)

Taiwan·Risk Class 1·MD·I DO BIOTECH CO., LTD.·Registered Jan 24, 2019 – Jan 24, 2024Expired

Registration details

Analysis ID: 4fbd8c13c8dab9a0e00c9bbccd2f5d7b
License Form: Ministry of Health Medical Device Import No. 020056
Customs Code: DHA09402005602

Company information

Manufacturer: I DO BIOTECH CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: CHENG WEI 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 24, 2019
Expiry Date: Jan 24, 2024

About this record

Access comprehensive regulatory information for "I DO" 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 4fbd8c13c8dab9a0e00c9bbccd2f5d7b and manufactured by I DO BIOTECH CO., LTD.. The authorized representative in Taiwan is CHENG WEI BIOTECH CO., LTD..

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