Taiwan FDA registration 93632e685911e5f211b045285cb051f1
"Termao" blood collection pen (unsterilized)
TW: “泰爾茂” 採血筆 (未滅菌)
Registration details
- Analysis ID
- 93632e685911e5f211b045285cb051f1
- Customs Code
- DHA09300864703
Company information
- Manufacturer Country
- Taiwan, Province of China;;Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Contract manufacturing;; Domestic;; Foreign commissioned domestic manufacturing, and then unified by foreign imports
Dates and status
- Registration Date
- Oct 20, 2020
- Expiry Date
- Oct 20, 2025
About this record
Access comprehensive regulatory information for "Termao" blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93632e685911e5f211b045285cb051f1 and manufactured by TERUMO CORPORATION;; Taibo Technology Co., Ltd. is a five-share plant. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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