Taiwan FDA registration 4b8e8cf4f09d0d4068be25ce4cdd798e

"Boston Tech" Libo hydrophilic wire

TW: “波士頓科技”利博親水性導線
Taiwan flagTaiwan·Risk Class 2·LAKE REGION MEDICAL·Registered Sep 03, 2007 – Sep 03, 2022Cancelled
Registration details
Analysis ID
4b8e8cf4f09d0d4068be25ce4cdd798e
Customs Code
DHA00601823201
Company information
Manufacturer Country
United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5130 泌尿導管及其附件
Import Information
import
Dates and status
Registration Date
Sep 03, 2007
Expiry Date
Sep 03, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Boston Tech" Libo hydrophilic wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b8e8cf4f09d0d4068be25ce4cdd798e and manufactured by LAKE REGION MEDICAL. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including LAKE REGION MEDICAL, Venusa de Mexico S de R.L. de C.V.;; Lake Region Medical, 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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