Taiwan FDA registration 1a37e8e127774e8df451c28ef80f8b3a
"Elekoda" thermocoagulation electrocauter
TW: "醫科達" 熱凝電燒灼器
Taiwan·Risk Class 2·ELEKTA INSTRUMENT AB·Registered Nov 07, 2005 – Nov 07, 2020CancelledRegistration details
- Analysis ID
- 1a37e8e127774e8df451c28ef80f8b3a
- Customs Code
- DHA00601295906
Company information
- Manufacturer
- ELEKTA INSTRUMENT AB
- Manufacturer Country
- Sweden
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4400 Shot Cutout Generator
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2005
- Expiry Date
- Nov 07, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Elekoda" thermocoagulation electrocauter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a37e8e127774e8df451c28ef80f8b3a and manufactured by ELEKTA INSTRUMENT AB. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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