Taiwan FDA registration b65dd30737d494add2cffba6b6ccb1cd
"Cottman" Fusatu discarded non-stick bipolar electrocauterizing device
TW: “柯特曼”芙莎圖拋棄式不沾黏雙極電燒器械
Taiwan·Risk Class 2·INTEGRA LIFESCIENCES SWITZERLAND SARL;; SUTTER MEDIZINTECHNIK GMBH·Registered Sep 06, 2022 – Sep 06, 2027ActiveRegistration details
- Analysis ID
- b65dd30737d494add2cffba6b6ccb1cd
- Customs Code
- DHA05603584205
Company information
- Manufacturer Country
- Germany;;Switzerland
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Sep 06, 2022
- Expiry Date
- Sep 06, 2027
About this record
Access comprehensive regulatory information for "Cottman" Fusatu discarded non-stick bipolar electrocauterizing device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b65dd30737d494add2cffba6b6ccb1cd and manufactured by INTEGRA LIFESCIENCES SWITZERLAND SARL;; SUTTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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