Taiwan FDA registration 6a4dec59ad7878daf9c2cac75c754b9d

"Boston Tech" Amberen subcutaneous electrode

TW: “波士頓科技”安博倫皮下電極
Taiwan flagTaiwan·Risk Class 3·OSCOR INC.·Registered Jul 31, 2017 – Jul 31, 2022Cancelled
Registration details
Analysis ID
6a4dec59ad7878daf9c2cac75c754b9d
Customs Code
DHA05603009100
Company information
Manufacturer
OSCOR INC.
Manufacturer Country
United States
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.3680 心血管用永久或暫時性之心律調節器電極
Import Information
Import;; Safety monitoring
Dates and status
Registration Date
Jul 31, 2017
Expiry Date
Jul 31, 2022
Cancellation Date
Mar 08, 2022
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Boston Tech" Amberen subcutaneous electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6a4dec59ad7878daf9c2cac75c754b9d and manufactured by OSCOR INC.. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Guidant Puerto Rico B.V., A Wholly Owned Subsidiary of Boston Scientific Corporation, and 1 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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