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"Sanyo" Enfi canal - Taiwan Registration cf9a3f843b2c7a285102a6813a8b9ca8

Access comprehensive regulatory information for "Sanyo" Enfi canal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf9a3f843b2c7a285102a6813a8b9ca8 and manufactured by SANYO POLYMER INDUSTRY CO., LTD.. The authorized representative in Taiwan is Huangfa Co., Ltd.

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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cf9a3f843b2c7a285102a6813a8b9ca8
Registration Details
Taiwan FDA Registration: cf9a3f843b2c7a285102a6813a8b9ca8
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Device Details

"Sanyo" Enfi canal
TW: "ไธ‰ๆด‹" ๆฉ่ฒ่‚›็ฎก
Risk Class 1
Cancelled

Registration Details

cf9a3f843b2c7a285102a6813a8b9ca8

DHA04400372401

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Gastrointestinal Tubes and Their Accessories (H.5980)".

H Gastroenterology and urology

H.5980 Gastric insulal tube and its accessories

import

Dates and Status

Apr 13, 2006

Apr 13, 2011

Oct 25, 2012

Cancellation Information

Logged out

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