Taiwan FDA registration 1b64c4a2560b767403210c635b5a04cd

Aeon CPKit

TW: 亞恩血球細胞分離器
Taiwan flagTaiwan·Risk Class 2·MD·AEON BIOTHERAPEUTICS CORP.·Registered Nov 26, 2015 – Nov 26, 2025Expired
Registration details
Analysis ID
1b64c4a2560b767403210c635b5a04cd
License Form
Ministry of Health Medical Device Manufacturing No. 004965
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
AEON BIOTHERAPEUTICS CORP.
Product details
Intended Use
This product can be used for blood collection and processing, blood is drawn from the patient, and autologous platelet rich plasma (PRP) is separated to prepare autologous platelet thick fluid (PRP).
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B9245 Automatic Hematology Cell Separator
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Nov 26, 2015
Expiry Date
Nov 26, 2025
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About this record

Access comprehensive regulatory information for Aeon CPKit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1b64c4a2560b767403210c635b5a04cd and manufactured by AEON BIOTHERAPEUTICS CORP.. The authorized representative in Taiwan is AEON BIOTHERAPEUTICS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AEON BIOTHERAPEUTICS CORP., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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