Taiwan FDA registration 893537058d27ac3f6381643fc495fd4d

"Denshi Pie Melfo" Putai U Root Tube Paper Needle (Unsterilized)

TW: "登士派麥樂佛" 普泰優根管紙針 (未滅菌)

Taiwan·Risk Class 1·DENTSPLY DENTAL (TIANJIN) CO., LTD.·Registered Apr 13, 2006 – Apr 13, 2011Expired

Registration details

Analysis ID: 893537058d27ac3f6381643fc495fd4d
Customs Code: DHA04400373809

Company information

Manufacturer: DENTSPLY DENTAL (TIANJIN) CO., LTD.
Manufacturer Country: China
Authorized Representative: Taiwan Branch of American Denspie Co., Ltd

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3830 Root Canal
Import Information: import

Dates and status

Registration Date: Apr 13, 2006
Expiry Date: Apr 13, 2011
Cancellation Date: May 09, 2011

About this record

Access comprehensive regulatory information for "Denshi Pie Melfo" Putai U Root Tube Paper Needle (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 893537058d27ac3f6381643fc495fd4d and manufactured by DENTSPLY DENTAL (TIANJIN) CO., LTD.. The authorized representative in Taiwan is Taiwan Branch of American Denspie Co., Ltd.

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