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"Boehringer" Cardiopulmonary bypass accessory equipment (Non-Sterile) - Taiwan Registration 9a5f564d2bb554b21a25329bce90c62b

Access comprehensive regulatory information for "Boehringer" Cardiopulmonary bypass accessory equipment (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a5f564d2bb554b21a25329bce90c62b and manufactured by Boehringer Laboratories, LLC. The authorized representative in Taiwan is FRIENDS SCIENTIFIC 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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9a5f564d2bb554b21a25329bce90c62b
Registration Details
Taiwan FDA Registration: 9a5f564d2bb554b21a25329bce90c62b
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Device Details

"Boehringer" Cardiopulmonary bypass accessory equipment (Non-Sterile)
TW: "ไผฏ็‘žๆ ผ" ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9a5f564d2bb554b21a25329bce90c62b

Ministry of Health Medical Device Import No. 017234

DHA09401723400

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).

E Cardiovascular devices

E4200 Cardiopulmonary vascular bypass assistive device

Imported from abroad

Dates and Status

Nov 30, 2016

Nov 30, 2026