Taiwan FDA registration 23b146be3e42f981e8b89d0d3aeeff18
“Needleless” Drug Preparation System and Needleless Injection Access Device
TW: “尼得立斯”藥物準備系統輸液接頭
Taiwan·Risk Class 2·MD·NEEDLELESS CORPORATION·Registered May 01, 2017 – May 01, 2027ActiveRegistration details
- Analysis ID
- 23b146be3e42f981e8b89d0d3aeeff18
- License Form
- Ministry of Health Medical Device Manufacturing No. 005723
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NEEDLELESS CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order. The additional specifications and indications were changed to: as detailed as Chinese the approved copy of the imitation order (the original approved copy of the imitation label approved on May 15, 106 is invalid).
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5440 Intravascular infusion sleeve
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 01, 2017
- Expiry Date
- May 01, 2027
About this record
Access comprehensive regulatory information for “Needleless” Drug Preparation System and Needleless Injection Access Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 23b146be3e42f981e8b89d0d3aeeff18 and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is NEEDLELESS CORPORATION.
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