Taiwan FDA registration 6f30b7fa9050e68d4654794aa19b4590
SIERS Treatment table (unsterilized)
TW: 席爾思 治療檯 (未滅菌)
Taiwan·Risk Class 1·SEERS MEDICAL LIMITED.·Registered Dec 29, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 6f30b7fa9050e68d4654794aa19b4590
- Customs Code
- DHA084a0014701
Company information
- Manufacturer
- SEERS MEDICAL LIMITED.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Treatment Table (O.3520)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3520 Therapeutic cage
Dates and status
- Registration Date
- Dec 29, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for SIERS Treatment table (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6f30b7fa9050e68d4654794aa19b4590 and manufactured by SEERS MEDICAL LIMITED.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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