Taiwan FDA registration 9a5f564d2bb554b21a25329bce90c62b

"Boehringer" Cardiopulmonary bypass accessory equipment (Non-Sterile)

TW: "伯瑞格" 心肺血管繞道術輔助設備 (未滅菌)

Taiwan·Risk Class 1·MD·Boehringer Laboratories, LLC·Registered Nov 30, 2016 – Nov 30, 2026Active

Registration details

Analysis ID: 9a5f564d2bb554b21a25329bce90c62b
License Form: Ministry of Health Medical Device Import No. 017234
Customs Code: DHA09401723400

Company information

Manufacturer: Boehringer Laboratories, LLC
Manufacturer Country: United States
Authorized Representative: FRIENDS SCIENTIFIC CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E4200 Cardiopulmonary vascular bypass assistive device
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 30, 2016
Expiry Date: Nov 30, 2026

About this record

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..

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