Taiwan FDA registration 5ddcb6be395f588f456f49628876325e
“GE” Giraffe Blue Spot PT Lite
TW: “奇異”新生兒光照射治療裝置
Taiwan·Risk Class 2·MD·Lumitex Medical Devices, Inc.·Registered Apr 18, 2017 – Apr 18, 2027ActiveRegistration details
- Analysis ID
- 5ddcb6be395f588f456f49628876325e
- License Form
- Ministry of Health Medical Device Import No. 029639
- Customs Code
- DHA05602963909
Company information
- Manufacturer
- Lumitex Medical Devices, 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)
- J5700 Neonatal Light Irradiation Therapy Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 18, 2017
- Expiry Date
- Apr 18, 2027
About this record
Access comprehensive regulatory information for “GE” Giraffe Blue Spot PT Lite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ddcb6be395f588f456f49628876325e and manufactured by Lumitex Medical Devices, Inc.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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