Taiwan FDA registration 4e23ac507b24863da108fb5d13b5f3b2
"Nipro" intravenous indwelling needle
TW: “尼普洛”靜脈留置針
Taiwan·Risk Class 2·NIPRO CORPORATION ODATE FACTORY·Registered Mar 06, 2009 – Mar 06, 2029ActiveRegistration details
- Analysis ID
- 4e23ac507b24863da108fb5d13b5f3b2
- Customs Code
- DHA00601969303
Company information
- Manufacturer
- NIPRO CORPORATION ODATE FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL 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.5570 Subcutaneous single-chamber needle
- Import Information
- import
Dates and status
- Registration Date
- Mar 06, 2009
- Expiry Date
- Mar 06, 2029
About this record
Access comprehensive regulatory information for "Nipro" intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e23ac507b24863da108fb5d13b5f3b2 and manufactured by NIPRO CORPORATION ODATE FACTORY. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
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