Taiwan FDA registration a4da8281749a585957d51118dab6ee75

“Keystone” Dental Hand Instrument (Non-Sterile)

TW: “金石”牙科手用器械 (未滅菌)　

Taiwan·Risk Class 1·MD·KEYSTONE DENTAL, INC.·Registered May 28, 2014 – May 28, 2024Expired

Registration details

Analysis ID: a4da8281749a585957d51118dab6ee75
License Form: Ministry of Health Medical Device Import No. 014177
Customs Code: DHA09401417702

Company information

Manufacturer: KEYSTONE DENTAL, 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 Hand Instruments (F.4565)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4565 Hand instruments for dental use
Import Information: Imported from abroad

Dates and status

Registration Date: May 28, 2014
Expiry Date: May 28, 2024

About this record

Access comprehensive regulatory information for “Keystone” Dental Hand Instrument (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 a4da8281749a585957d51118dab6ee75 and manufactured by KEYSTONE DENTAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..

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