Taiwan FDA registration 0fe1e8739d7f4eac17a6b9fbe0dc279b
“RegenLab”RegenACR-C Classic Type III
TW: “利奇”艾奇爾經典第三型血球細胞分離套組
Taiwan·Risk Class 2·MD·REGEN LAB SA·Registered May 03, 2019 – May 03, 2024ExpiredRegistration details
- Analysis ID
- 0fe1e8739d7f4eac17a6b9fbe0dc279b
- License Form
- Ministry of Health Medical Device Import No. 032418
- Customs Code
- DHA05603241803
Company information
- Manufacturer
- REGEN LAB SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- This product is suitable for the preparation of Platelet-rich plasma (PRP), which can be used to treat chronic wounds.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9245 Automatic Hematology Cell Separator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 03, 2019
- Expiry Date
- May 03, 2024
About this record
Access comprehensive regulatory information for “RegenLab”RegenACR-C Classic Type III in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fe1e8739d7f4eac17a6b9fbe0dc279b and manufactured by REGEN LAB SA. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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