Taiwan FDA registration f7b2faf5f68d85e3ec1399dc3752441e

Sanyo wrist electronic blood pressure monitor

TW: 三洋腕式電子血壓計
Taiwan flagTaiwan·Risk Class 2·AVITA CORPORATION·Registered Sep 21, 2012 – Sep 21, 2017Cancelled
Registration details
Analysis ID
f7b2faf5f68d85e3ec1399dc3752441e
Company information
Manufacturer
AVITA CORPORATION
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Taiwan Sanyo Electric Co., Ltd
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1130.
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Sep 21, 2012
Expiry Date
Sep 21, 2017
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Sanyo wrist 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 f7b2faf5f68d85e3ec1399dc3752441e 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 2 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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