Taiwan FDA registration 2b9c9d0cadcc6891e6bf052afbb91ef6
“Hologic”Specimen Radiography System
TW: “豪洛捷”標本X光影像系統
Taiwan·Risk Class 2·MD·Hologic, Inc.·Registered Mar 18, 2022 – Mar 18, 2027ActiveRegistration details
- Analysis ID
- 2b9c9d0cadcc6891e6bf052afbb91ef6
- License Form
- Ministry of Health Medical Device Import No. 035336
- Customs Code
- DHAS5603533601
Company information
- Manufacturer
- Hologic, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P1680 stationary X-ray system
- Import Information
- Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)
Dates and status
- Registration Date
- Mar 18, 2022
- Expiry Date
- Mar 18, 2027
About this record
Access comprehensive regulatory information for “Hologic”Specimen Radiography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b9c9d0cadcc6891e6bf052afbb91ef6 and manufactured by Hologic, Inc.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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