Taiwan FDA registration 0991124e20be6c98869187195a4efe7c

Vitrolife Micromanipulation Pipettes

TW: 密陀來福體外受精顯微操作管
Taiwan flagTaiwan·Risk Class 2·MD·Vitrolife Inc.·Registered Feb 26, 2015 – Feb 26, 2025Expired
Registration details
Analysis ID
0991124e20be6c98869187195a4efe7c
License Form
Ministry of Health Medical Device Import No. 027027
Customs Code
DHA05602702707
Company information
Manufacturer
Vitrolife Inc.
Manufacturer Country
United States
Authorized Representative
TSENG HSIANG LIFE SCIENCE LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
l Devices for obstetrics and gynecology
Product Type (Level 2)
L6130 Tiny apparatus for assisted reproduction
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 26, 2015
Expiry Date
Feb 26, 2025
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About this record

Access comprehensive regulatory information for Vitrolife Micromanipulation Pipettes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0991124e20be6c98869187195a4efe7c and manufactured by Vitrolife Inc.. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Vitrolife Sweden AB, 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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