Taiwan FDA registration bb8adef291aec93668c99f6958dce14b

"Ronamac" Antistammering device (Non-Sterile)

TW: "朋笛"口吃矯正器材(未滅菌)

Taiwan·Risk Class 1·MD·ARTICULATE INSTRUMENTS LTD.·Registered Jul 26, 2018 – Jul 26, 2023Expired

Registration details

Analysis ID: bb8adef291aec93668c99f6958dce14b
License Form: Ministry of Health Medical Device Import No. 019419
Customs Code: DHA09401941909

Company information

Manufacturer: ARTICULATE INSTRUMENTS LTD.
Manufacturer Country: United Kingdom
Authorized Representative: RONAMAC INTERNATIONAL CORP.

Product details

Intended Use: Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Stuttering Correction Equipment (G.5840)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G5840 Stutter correction device
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 26, 2018
Expiry Date: Jul 26, 2023

About this record

Access comprehensive regulatory information for "Ronamac" Antistammering device (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 bb8adef291aec93668c99f6958dce14b and manufactured by ARTICULATE INSTRUMENTS LTD.. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..

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