Taiwan FDA registration 1d20747c5ad2388167efe8560fef0d49
"Lenette" alternating pressure air mattress (unsterilized)
TW: "萊內特" 交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·LINET SPOL. S R. O.·Registered Jan 12, 2023 – Jan 12, 2028ActiveRegistration details
- Analysis ID
- 1d20747c5ad2388167efe8560fef0d49
- Customs Code
- DHA09402301207
Company information
- Manufacturer
- LINET SPOL. S R. O.
- Manufacturer Country
- Czechia
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 12, 2023
- Expiry Date
- Jan 12, 2028
About this record
Access comprehensive regulatory information for "Lenette" 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 1d20747c5ad2388167efe8560fef0d49 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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