Taiwan FDA registration 7f9cdf6a55175b44e3d81fce6d636d30
"Stryker" Sleep Surface (Non-Sterile)
TW: "史賽克" 非動力式治療床墊 (未滅菌)
Taiwan·Risk Class 1·MD·STRYKER MEDICAL·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 7f9cdf6a55175b44e3d81fce6d636d30
- License Form
- Ministry of Health Medical Device Import Registration No. 002524
- Customs Code
- DHA08400252408
Company information
- Manufacturer
- STRYKER MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Has the function of supporting the patient to prevent excessive stress on the part of the body. This device can be used to treat or avoid bedsores caused by bed rest.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Stryker" Sleep Surface (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 7f9cdf6a55175b44e3d81fce6d636d30 and manufactured by STRYKER MEDICAL. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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