Taiwan FDA registration 3e237a1f205c4204238ec039ed90a7cf
“GE” Probe for medical use
TW: “奇異”診斷用超音波探頭
Taiwan·Risk Class 2·MD·GE Healthcare Japan Corporation·Registered Dec 15, 2017 – Dec 15, 2027ActiveRegistration details
- Analysis ID
- 3e237a1f205c4204238ec039ed90a7cf
- License Form
- Ministry of Health Medical Device Import No. 030616
- Customs Code
- DHA05603061600
Company information
- Manufacturer
- GE Healthcare Japan Corporation
- Manufacturer Country
- Japan
- 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)
- P Devices for radiology
- Product Type (Level 2)
- P1570 Ultrasound converter for diagnostics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 15, 2017
- Expiry Date
- Dec 15, 2027
About this record
Access comprehensive regulatory information for “GE” Probe for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e237a1f205c4204238ec039ed90a7cf and manufactured by GE Healthcare Japan Corporation. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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