Taiwan FDA registration 8c1da723e71fc7c82cbe1262142d6e88
"Lenet" non-powered treatment mattress (unsterilized)
TW: “萊內特” 非動力式治療床墊 (未滅菌)
Taiwan·Risk Class 1·LINET SPOL. S R. O.·Registered Oct 15, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 8c1da723e71fc7c82cbe1262142d6e88
- Customs Code
- DHA084a0012402
Company information
- Manufacturer
- LINET SPOL. S R. O.
- Manufacturer Country
- Czechia
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "Non-powered floating therapy mattress (J.5150)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5150 Non-powered floating therapy mattress
Dates and status
- Registration Date
- Oct 15, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Lenet" non-powered treatment 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 8c1da723e71fc7c82cbe1262142d6e88 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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