Taiwan FDA registration 4534b964f37248b55afe7fe40b1f3cd3
Griflex infusion bags
TW: 基立福適輸液袋
Taiwan·Risk Class 2·Laboratorios Grifols, S.A.·Registered Dec 26, 2008 – Dec 26, 2018CancelledRegistration details
- Analysis ID
- 4534b964f37248b55afe7fe40b1f3cd3
- Customs Code
- DHA00601953501
Company information
- Manufacturer
- Laboratorios Grifols, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- TAIWAN GREEN CROSS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5025 靜脈輸液用容器
- Import Information
- import
Dates and status
- Registration Date
- Dec 26, 2008
- Expiry Date
- Dec 26, 2018
- Cancellation Date
- Dec 24, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Griflex infusion bags in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4534b964f37248b55afe7fe40b1f3cd3 and manufactured by Laboratorios Grifols, S.A.. The authorized representative in Taiwan is TAIWAN GREEN CROSS CO., LTD..
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