Taiwan FDA registration 11d5f12b9d2932f962dee9d5921d06b9

Aeon CPKit

TW: 亞恩骨髓濃厚液分離器
Taiwan flagTaiwan·Risk Class 2·MD·AEON BIOTHERAPEUTICS CORP.·Registered May 04, 2016 – May 04, 2026Expired
Registration details
Analysis ID
11d5f12b9d2932f962dee9d5921d06b9
License Form
Ministry of Health Medical Device Manufacturing No. 005171
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
AEON BIOTHERAPEUTICS CORP.
Product details
Intended Use
This product is used with a centrifuge system to prepare Bone Marrow Concentrate (BMC) from bone marrow separation in clinical examination rooms or surgery.
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
May 04, 2016
Expiry Date
May 04, 2026
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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 11d5f12b9d2932f962dee9d5921d06b9 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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