Taiwan FDA registration 23353410213c59b0d4f7e15a22a084ef
"Carestream" Radiographic film (Non-Sterile)
TW: "康世" 放射線影片 (未滅菌)
Registration details
- Analysis ID
- 23353410213c59b0d4f7e15a22a084ef
- License Form
- Ministry of Health Medical Device Import No. 018489
- Customs Code
- DHA09401848902
Company information
- Manufacturer
- CARESTREAM HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FAITH BIOMED LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1840 Radiographic video
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 13, 2017
- Expiry Date
- Nov 13, 2022
About this record
Access comprehensive regulatory information for "Carestream" Radiographic film (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23353410213c59b0d4f7e15a22a084ef and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED LTD..
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