Taiwan FDA registration b08d33c8b86932538e49a0f70eae8c41
"Karlsted" electronic mediastinoscope
TW: “卡爾斯特”電子式縱膈腔鏡
Taiwan·Risk Class 2·Karl Storz SE & Co. KG·Registered Jan 04, 2022 – Jan 04, 2027ActiveRegistration details
- Analysis ID
- b08d33c8b86932538e49a0f70eae8c41
- Customs Code
- DHA05603517100
Company information
- Manufacturer
- Karl Storz SE & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- KARL STORZ ENDOSCOPY TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4720 Diaphragmatic cavity mirrors and accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 04, 2022
- Expiry Date
- Jan 04, 2027
About this record
Access comprehensive regulatory information for "Karlsted" electronic mediastinoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b08d33c8b86932538e49a0f70eae8c41 and manufactured by Karl Storz SE & Co. KG. The authorized representative in Taiwan is KARL STORZ ENDOSCOPY TAIWAN LTD..
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