Taiwan FDA registration 38a0e94c85d5cb550fb8bff2d1e5e981
"Tessy" alternating pressure mattress (unsterilized)
TW: “泰希”交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·THE SURGICAL COMPANY INTERNATIONAL B. V.·Registered May 18, 2012 – May 18, 2022CancelledRegistration details
- Analysis ID
- 38a0e94c85d5cb550fb8bff2d1e5e981
- Customs Code
- DHA04401172203
Company information
- Manufacturer
- THE SURGICAL COMPANY INTERNATIONAL B. V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5550 交替式壓力氣墊床
- Import Information
- import
Dates and status
- Registration Date
- May 18, 2012
- Expiry Date
- May 18, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tessy" alternating pressure mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38a0e94c85d5cb550fb8bff2d1e5e981 and manufactured by THE SURGICAL COMPANY INTERNATIONAL B. V.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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