Taiwan FDA registration 93d97776be283a9847f06204ce6891f3
“AD-TECH” Stereotaxic Instrument
TW: “艾迪鈦克”立體定位手術用器械
Taiwan·Risk Class 2·MD·AD-TECH MEDICAL INSTRUMENT CORPORATION·Registered Nov 28, 2017 – Nov 28, 2027ActiveRegistration details
- Analysis ID
- 93d97776be283a9847f06204ce6891f3
- License Form
- Ministry of Health Medical Device Import No. 030569
- Customs Code
- DHA05603056901
Company information
- Manufacturer
- AD-TECH MEDICAL INSTRUMENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K4560 Instrument for stereotaxic use in the nervous system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 28, 2017
- Expiry Date
- Nov 28, 2027
About this record
Access comprehensive regulatory information for “AD-TECH” Stereotaxic Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 93d97776be283a9847f06204ce6891f3 and manufactured by AD-TECH MEDICAL INSTRUMENT CORPORATION. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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