Taiwan FDA registration aab4e0b8d4229936996975303fd98e5d

"Biomate" Endosseous dental implant accessory (Non-Sterile)

TW: "京達" 牙科植體附件 (未滅菌)

Taiwan·Risk Class 1·MD·F.F.D.M. PNEUMAT·Registered Apr 18, 2016 – Apr 18, 2026Expired

Registration details

Analysis ID: aab4e0b8d4229936996975303fd98e5d
License Form: Ministry of Health Medical Device Import No. 016411
Customs Code: DHA09401641104

Company information

Manufacturer: F.F.D.M. PNEUMAT
Manufacturer Country: France
Authorized Representative: BIOMATE MEDICAL DEVICES TECHNOLOGY 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: Apr 18, 2016
Expiry Date: Apr 18, 2026

About this record

Access comprehensive regulatory information for "Biomate" Endosseous dental implant accessory (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 aab4e0b8d4229936996975303fd98e5d and manufactured by F.F.D.M. PNEUMAT. The authorized representative in Taiwan is BIOMATE MEDICAL DEVICES TECHNOLOGY CO., LTD..

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