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"Deutschland" 5th generation automatic plasma pressure platen system - Taiwan Registration 67b70d80dd2f91b7dac1756763745065

Access comprehensive regulatory information for "Deutschland" 5th generation automatic plasma pressure platen system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67b70d80dd2f91b7dac1756763745065 and manufactured by FRESENIUS KABI AG;; SANMINA-SCI. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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67b70d80dd2f91b7dac1756763745065
Registration Details
Taiwan FDA Registration: 67b70d80dd2f91b7dac1756763745065
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Device Details

"Deutschland" 5th generation automatic plasma pressure platen system
TW: โ€œๅพทๆ„ๅฟ—โ€็ฌฌไบ”ไปฃ่‡ชๅ‹•่ก€ๆผฟๅฃ“ๆฟ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

67b70d80dd2f91b7dac1756763745065

DHA00602329608

Company Information

Sweden;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

B Hematology, pathology, and genetics

B.0002 Blood Component Extraction Apparatus

Contract manufacturing;; input

Dates and Status

Mar 06, 2012

Mar 06, 2022

Apr 12, 2024

Cancellation Information

Logged out

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