"SMEK" Cold Light Meter (Unsterilized)
Taiwan·Risk Class 1·Spectral Medical Inc.·Registered Apr 29, 2020 – Apr 29, 2025Cancelled- Analysis ID
- d0bdad625831444e356645d3f1e3a60b
- Customs Code
- DHA09402149402
- Manufacturer
- Spectral Medical Inc.
- Manufacturer Country
- Canada
- Authorized Representative
- HI-CLEARANCE INC.
- Intended Use
- Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- Input;; QMS/QSD
- Registration Date
- Apr 29, 2020
- Expiry Date
- Apr 29, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "SMEK" Cold Light Meter (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d0bdad625831444e356645d3f1e3a60b and manufactured by Spectral Medical Inc.. The authorized representative in Taiwan is HI-CLEARANCE INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Spectral Medical Inc., and 1 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.