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Aeon CPKit - Taiwan Registration 11d5f12b9d2932f962dee9d5921d06b9

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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11d5f12b9d2932f962dee9d5921d06b9
Registration Details
Taiwan FDA Registration: 11d5f12b9d2932f962dee9d5921d06b9
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Device Details

Aeon CPKit
TW: ไบžๆฉ้ชจ้ซ“ๆฟƒๅŽšๆถฒๅˆ†้›ขๅ™จ
Risk Class 2
MD

Registration Details

11d5f12b9d2932f962dee9d5921d06b9

Ministry of Health Medical Device Manufacturing No. 005171

Company Information

Taiwan, Province of China

Product Details

This product is used with a centrifuge system to prepare Bone Marrow Concentrate (BMC) from bone marrow separation in clinical examination rooms or surgery.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Produced in Taiwan, China

Dates and Status

May 04, 2016

May 04, 2026

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