Taiwan FDA registration 673181c2cb7fd6b78f6813463229db5e
"Lina" Liberta endometrial ablator
TW: “利拿”莉柏塔子宮內膜消融器
Taiwan·Risk Class 2·LiNA Medical Polska sp.z.o.o.;; LINA MEDICAL APS·Registered Oct 04, 2018 – Oct 04, 2028ActiveRegistration details
- Analysis ID
- 673181c2cb7fd6b78f6813463229db5e
- Customs Code
- DHA05603154709
Company information
- Manufacturer
- LiNA Medical Polska sp.z.o.o.;; LINA MEDICAL APS
- Manufacturer Country
- Poland;;Denmark
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.9999 Miscellaneous
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2018
- Expiry Date
- Oct 04, 2028
About this record
Access comprehensive regulatory information for "Lina" Liberta endometrial ablator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 673181c2cb7fd6b78f6813463229db5e and manufactured by LiNA Medical Polska sp.z.o.o.;; LINA MEDICAL APS. The authorized representative in Taiwan is Huizhong Co., Ltd.
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