Taiwan FDA registration c169f74f8b2f8599e268c01b57c9f17a

"Deutsche Boi" Ultrasonic Spray Therapy Accessory Kit (Unsterilized)

TW: "德國博依" 超音波噴霧治療器配件包 (未滅菌)

Taiwan·Risk Class 1·BEURER GMBH·Registered Oct 20, 2016 – Oct 20, 2021Cancelled

Registration details

Analysis ID: c169f74f8b2f8599e268c01b57c9f17a
Customs Code: DHA09401710107

Company information

Manufacturer: BEURER GMBH
Manufacturer Country: Germany
Authorized Representative: BIOWELL HEALTH & WELL-BEING INC.

Product details

Intended Use: Limited to the first level identification range of "oxygen mask (D.5580)", "breathing mouthpiece (D.5620)", "airway connector (D.5810)" and "liquid drug dispenser (J.6430)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5810 Air channel connectors;; D.5580 Oxygen masks;; D.5620 Breathing mouthpiece
Import Information: import

Dates and status

Registration Date: Oct 20, 2016
Expiry Date: Oct 20, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Deutsche Boi" Ultrasonic Spray Therapy Accessory Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c169f74f8b2f8599e268c01b57c9f17a and manufactured by BEURER GMBH. The authorized representative in Taiwan is BIOWELL HEALTH & WELL-BEING INC..

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