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Sanyo arm type electronic blood pressure monitor - Taiwan Registration fdb017923dca2510addbfb4039ce1eba

Access comprehensive regulatory information for Sanyo arm type electronic blood pressure monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdb017923dca2510addbfb4039ce1eba and manufactured by AVITA CORPORATION. The authorized representative in Taiwan is Taiwan Sanyo Electric Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AVITA CORPORATION, and 3 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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fdb017923dca2510addbfb4039ce1eba
Registration Details
Taiwan FDA Registration: fdb017923dca2510addbfb4039ce1eba
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Device Details

Sanyo arm type electronic blood pressure monitor
TW: ไธ‰ๆด‹่‡‚ๅผ้›ปๅญ่ก€ๅฃ“่จˆ
Risk Class 2
Cancelled

Registration Details

fdb017923dca2510addbfb4039ce1eba

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular Medicine Science

E.1130.

Contract manufacturing;; Domestic

Dates and Status

Dec 28, 2012

Dec 28, 2017

Dec 20, 2019

Cancellation Information

Logged out

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