Taiwan FDA registration 2071bd339796013bdb7543c3f697c733
“Baylis” NRG Transseptal Needle
TW: “貝利斯”心房中膈穿刺針
Taiwan·Risk Class 2·MD·BAYLIS MEDICAL COMPANY INC.·Registered Oct 07, 2019 – Oct 07, 2024ExpiredRegistration details
- Analysis ID
- 2071bd339796013bdb7543c3f697c733
- License Form
- Ministry of Health Medical Device Import No. 032894
- Customs Code
- DHA05603289409
Company information
- Manufacturer
- BAYLIS MEDICAL COMPANY INC.
- Manufacturer Country
- Canada
- Authorized Representative
- WIN CHAMP MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5175 Middle diaphragmectom catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 07, 2019
- Expiry Date
- Oct 07, 2024
About this record
Access comprehensive regulatory information for “Baylis” NRG Transseptal Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2071bd339796013bdb7543c3f697c733 and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is WIN CHAMP MEDICAL CO., LTD..
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