Taiwan FDA registration 6d19a86cb013a8e38f439167e8c1a321
"Apollo Endosurgery" Manual surgical instrument for general use (Non-Sterile)
TW: "阿波羅恩朵" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·APOLLO ENDOSURGERY, INC.·Registered Jan 13, 2017 – Jan 13, 2022ExpiredRegistration details
- Analysis ID
- 6d19a86cb013a8e38f439167e8c1a321
- License Form
- Ministry of Health Medical Device Import No. 017412
- Customs Code
- DHA09401741201
Company information
- Manufacturer
- APOLLO ENDOSURGERY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ERA BIOTEQ ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 13, 2017
- Expiry Date
- Jan 13, 2022
About this record
Access comprehensive regulatory information for "Apollo Endosurgery" Manual surgical instrument for general use (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 6d19a86cb013a8e38f439167e8c1a321 and manufactured by APOLLO ENDOSURGERY, INC.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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