Taiwan FDA registration 69da72d6e7fe77ef1a99a87a5ba1860c
"Termao" arterial sampler (sterilized)
TW: "泰爾茂" 動脈取樣器(滅菌)
Taiwan·Risk Class 1·TERUMO CORPORATION;; KOFU FACTORY OF TERUMO CORPORATION·Registered Mar 29, 2005 – Mar 29, 2020CancelledRegistration details
- Analysis ID
- 69da72d6e7fe77ef1a99a87a5ba1860c
- Customs Code
- DHA04400001404
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- It is used to draw blood from the arteries for blood qi measurement.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.1100 動脈血液取樣組
- Import Information
- import
Dates and status
- Registration Date
- Mar 29, 2005
- Expiry Date
- Mar 29, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Termao" arterial sampler (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 69da72d6e7fe77ef1a99a87a5ba1860c and manufactured by TERUMO CORPORATION;; KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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