Taiwan FDA registration 41a8c629ad110d273c769ce785f535e5

“GE” Neonatal Incubator

TW: “奇異”新生兒保溫箱
Taiwan flagTaiwan·Risk Class 2·MD·DATEX-OHMEDA INC.·Registered Nov 25, 2016 – Nov 25, 2026Active
Registration details
Analysis ID
41a8c629ad110d273c769ce785f535e5
License Form
Ministry of Health Medical Device Import No. 029075
Customs Code
DHA05602907502
Company information
Manufacturer
DATEX-OHMEDA INC.
Manufacturer Country
United States
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, 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)
J5400 Neonatal incubator
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 25, 2016
Expiry Date
Nov 25, 2026
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About this record

Access comprehensive regulatory information for “GE” Neonatal Incubator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41a8c629ad110d273c769ce785f535e5 and manufactured by DATEX-OHMEDA INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Wipro GE Healthcare Pvt. Ltd., 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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