Taiwan FDA registration 3ec551847b18381c2eeef0b0d2a4e336

"Natex" neonatal jaundice phototherapy instrument

TW: “納特士”新生兒黃疸光療儀
Taiwan flagTaiwan·Risk Class 2·Natus Medical Incorporated·Registered Mar 19, 2013 – Mar 19, 2018Cancelled
Registration details
Analysis ID
3ec551847b18381c2eeef0b0d2a4e336
Customs Code
DHA00602459102
Company information
Manufacturer Country
United States
Authorized Representative
WISDOM UNION ENTERPRISE CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5700 Neonatal light therapy device
Import Information
import
Dates and status
Registration Date
Mar 19, 2013
Expiry Date
Mar 19, 2018
Cancellation Date
Dec 13, 2019
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 "Natex" neonatal jaundice phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ec551847b18381c2eeef0b0d2a4e336 and manufactured by Natus Medical Incorporated. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Natus Medical Incorporated DBA Excel-Tech Ltd. (XLTEK), 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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