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"Deutsche Boi" Ultrasonic Spray Therapy Accessory Kit (Unsterilized) - Taiwan Registration c169f74f8b2f8599e268c01b57c9f17a

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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c169f74f8b2f8599e268c01b57c9f17a
Registration Details
Taiwan FDA Registration: c169f74f8b2f8599e268c01b57c9f17a
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Device Details

"Deutsche Boi" Ultrasonic Spray Therapy Accessory Kit (Unsterilized)
TW: "ๅพทๅœ‹ๅšไพ" ่ถ…้Ÿณๆณขๅ™ด้œงๆฒป็™‚ๅ™จ้…ไปถๅŒ… (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c169f74f8b2f8599e268c01b57c9f17a

DHA09401710107

Company Information

Germany

Product Details

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.

D Anesthesiology

D.5810 Air channel connectors;; D.5580 Oxygen masks;; D.5620 Breathing mouthpiece

import

Dates and Status

Oct 20, 2016

Oct 20, 2021

Sep 23, 2023

Cancellation Information

Logged out

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