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Sanyo arm type electronic blood pressure monitor - Taiwan Registration c0d64a0a5f5c854599e82fc196620207

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 c0d64a0a5f5c854599e82fc196620207 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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c0d64a0a5f5c854599e82fc196620207
Registration Details
Taiwan FDA Registration: c0d64a0a5f5c854599e82fc196620207
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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

c0d64a0a5f5c854599e82fc196620207

DHY00500337501

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.

Domestic;; Contract manufacturing

Dates and Status

Jul 01, 2011

Jul 01, 2021

Sep 19, 2023

Cancellation Information

Logged out

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