Taiwan FDA registration 1ef00f87128fafd956f9ce9a69137432
"Linet" Powered patient rotation bed (Non-Sterile)
TW: "里內特" 動力式病人翻身床 (未滅菌)
Taiwan·Risk Class 1·MD·LINET SPOL. S R. O.·Registered Aug 28, 2015 – Aug 28, 2020CancelledRegistration details
- Analysis ID
- 1ef00f87128fafd956f9ce9a69137432
- License Form
- Ministry of Health Medical Device Import No. 015619
- Customs Code
- DHA09401561900
Company information
- Manufacturer
- LINET SPOL. S R. O.
- Manufacturer Country
- Czechia
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5225 Power Patient Rollover Bed
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 28, 2015
- Expiry Date
- Aug 28, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Linet" Powered patient rotation bed (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 1ef00f87128fafd956f9ce9a69137432 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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