Taiwan FDA registration 549c092d88afecd3ed6919261668a356
"Navak" alternating pressure air mattress (unsterilized)
TW: “娜瓦克”交替式壓力氣墊床 (未滅菌)
Taiwan·Risk Class 1·NOVACARE GMBH·Registered Apr 30, 2013 – Apr 30, 2018CancelledRegistration details
- Analysis ID
- 549c092d88afecd3ed6919261668a356
- Customs Code
- DHA04401295403
Company information
- Manufacturer
- NOVACARE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SEQUOIA-TWN HEALTHCARE CO., 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
- Apr 30, 2013
- Expiry Date
- Apr 30, 2018
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Navak" alternating pressure air 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 549c092d88afecd3ed6919261668a356 and manufactured by NOVACARE GMBH. The authorized representative in Taiwan is SEQUOIA-TWN HEALTHCARE CO., LTD..
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