Taiwan FDA registration 74853f37bb320441c013790bc0dc4042
"Flex" endoscope accessory (sterilization)
TW: "福萊克斯" 內視鏡附件 (滅菌)
Taiwan·Risk Class 1·ENDO-FLEX GmbH·Registered Aug 04, 2015 – Aug 04, 2025ExpiredRegistration details
- Analysis ID
- 74853f37bb320441c013790bc0dc4042
- Customs Code
- DHA09401555102
Company information
- Manufacturer
- ENDO-FLEX GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 04, 2015
- Expiry Date
- Aug 04, 2025
About this record
Access comprehensive regulatory information for "Flex" endoscope accessory (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74853f37bb320441c013790bc0dc4042 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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