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Aeon CPKit - Taiwan Registration 1b64c4a2560b767403210c635b5a04cd

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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1b64c4a2560b767403210c635b5a04cd
Registration Details
Taiwan FDA Registration: 1b64c4a2560b767403210c635b5a04cd
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Device Details

Aeon CPKit
TW: ไบžๆฉ่ก€็ƒ็ดฐ่ƒžๅˆ†้›ขๅ™จ
Risk Class 2
MD

Registration Details

1b64c4a2560b767403210c635b5a04cd

Ministry of Health Medical Device Manufacturing No. 004965

Company Information

Taiwan, Province of China

Product Details

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).

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Produced in Taiwan, China

Dates and Status

Nov 26, 2015

Nov 26, 2025

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