Taiwan FDA registration 17559c612fb63ef089afc6c900b69bf8
“Apollo Endosurgery” OverStitch Endoscopic Suturing System
TW: “阿波羅恩朵”內視鏡縫線系統
Taiwan·Risk Class 2·MD·APOLLO ENDOSURGERY, INC.·Registered Dec 10, 2018 – Dec 10, 2028ActiveRegistration details
- Analysis ID
- 17559c612fb63ef089afc6c900b69bf8
- License Form
- Ministry of Health Medical Device Import No. 031918
- Customs Code
- DHA05603191805
Company information
- Manufacturer
- APOLLO ENDOSURGERY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ERA BIOTEQ ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 10, 2018
- Expiry Date
- Dec 10, 2028
About this record
Access comprehensive regulatory information for “Apollo Endosurgery” OverStitch Endoscopic Suturing System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17559c612fb63ef089afc6c900b69bf8 and manufactured by APOLLO ENDOSURGERY, INC.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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