Taiwan FDA registration 6478efb7557878bede0be48b815fed8d

“Rhinolab” Oxygen mask (Non-Sterile)

TW: “萊諾錸博” 氧氣面罩 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RHINOLAB GMBH·Registered Jul 26, 2018 – Jul 26, 2023Cancelled
Registration details
Analysis ID
6478efb7557878bede0be48b815fed8d
License Form
Ministry of Health Medical Device Import No. 019420
Customs Code
DHA09401942007
Company information
Manufacturer
RHINOLAB GMBH
Manufacturer Country
Germany
Authorized Representative
BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5580 oxygen mask
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 26, 2018
Expiry Date
Jul 26, 2023
Cancellation Date
Jan 10, 2020
Cancellation information
Status
Logged out
Reason
自請註銷
About this record

Access comprehensive regulatory information for “Rhinolab” Oxygen mask (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 6478efb7557878bede0be48b815fed8d and manufactured by RHINOLAB GMBH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

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.

Free DatabasePowered by Pure Global AI89,000+ Devices