Taiwan FDA registration 6a053eebcae2bcbcc48deff3eee790ea
"Stryker" Alternating pressure air flotation mattress (Non-Sterile)
TW: "史泰克"交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·MD·STRYKER MEDICAL·Registered Apr 07, 2015 – Apr 07, 2020CancelledRegistration details
- Analysis ID
- 6a053eebcae2bcbcc48deff3eee790ea
- License Form
- Ministry of Health Medical Device Import No. 015076
- Customs Code
- DHA09401507601
Company information
- Manufacturer
- STRYKER MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- Meide Medical Devices Co., Ltd
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5550 Alternating pressure air mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 07, 2015
- Expiry Date
- Apr 07, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Stryker" Alternating pressure air flotation mattress (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 6a053eebcae2bcbcc48deff3eee790ea and manufactured by STRYKER MEDICAL. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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