"Singular" ultrasound system
- Analysis ID
- 57daaf692f4ee790f6d2963509846da1
- Customs Code
- DHA00602207401
- Manufacturer
- WIPRO GE HEALTHCARE PVT. LTD.
- Manufacturer Country
- India
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Feb 26, 2011
- Expiry Date
- Feb 26, 2021
- Cancellation Date
- Sep 23, 2023
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Singular" ultrasound system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57daaf692f4ee790f6d2963509846da1 and manufactured by WIPRO GE HEALTHCARE PVT. LTD.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including GE VINGMED ULTRASOUND AS, GE Medical Systems Israel Ltd., and 5 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.