Taiwan FDA registration 5f691710688027a1e16990caca3cf803

Double the root tube paper needle

TW: 加倍登根管紙針

Taiwan·Risk Class 1·GAPADENT CO., LTD.·Registered Apr 10, 2006 – Apr 10, 2011Cancelled

Registration details

Analysis ID: 5f691710688027a1e16990caca3cf803
Customs Code: DHA04400355208

Company information

Manufacturer: GAPADENT CO., LTD.
Manufacturer Country: Canada
Authorized Representative: C&N MED-DENT CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Administrative Measures for Medical Devices (Root Tube Paper Needle [F.3830]).
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3820 根管充填樹脂
Import Information: import

Dates and status

Registration Date: Apr 10, 2006
Expiry Date: Apr 10, 2011
Cancellation Date: Nov 05, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Double the root tube paper needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f691710688027a1e16990caca3cf803 and manufactured by GAPADENT CO., LTD.. The authorized representative in Taiwan is C&N MED-DENT CO., LTD..

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