Taiwan FDA registration 5f940bade6eb72541416e3f648545ac8
"Shinto" vacuum drawing bottle
TW: “信東”真空引流瓶
Taiwan·Risk Class 1·TAIWAN BIOTECH CO., LTD.·Registered Jul 14, 2006 – Jul 14, 2016CancelledRegistration details
- Analysis ID
- 5f940bade6eb72541416e3f648545ac8
Company information
- Manufacturer
- TAIWAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN BIOTECH CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of the Administrative Measures for Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Jul 14, 2006
- Expiry Date
- Jul 14, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Shinto" vacuum drawing bottle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f940bade6eb72541416e3f648545ac8 and manufactured by TAIWAN BIOTECH CO., LTD.. The authorized representative in Taiwan is TAIWAN BIOTECH 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