Taiwan FDA registration 0a5ec171c6bcff41bcc5c89f1d1dab93
"Snygis" Marys bipolar electrofiring system
TW: “史奈吉斯”瑪里士雙極電燒系統
Taiwan·Risk Class 2·SYNERGETICS, INC.·Registered Nov 25, 2008 – Nov 25, 2013CancelledRegistration details
- Analysis ID
- 0a5ec171c6bcff41bcc5c89f1d1dab93
- Customs Code
- DHA00601937107
Company information
- Manufacturer
- SYNERGETICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Nov 25, 2008
- Expiry Date
- Nov 25, 2013
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Snygis" Marys bipolar electrofiring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a5ec171c6bcff41bcc5c89f1d1dab93 and manufactured by SYNERGETICS, INC.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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