Taiwan FDA registration bdc0e08877943b140b2ac019c6451670

"SMEK" Cold Light Meter (Unsterilized)

TW: “思邁克”冷光儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Spectral Medical Inc.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
bdc0e08877943b140b2ac019c6451670
Customs Code
DHA08402149406
Company information
Manufacturer Country
Canada
Authorized Representative
HI-CLEARANCE INC.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Classification and Grading of Medical Devices "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)".
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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 bdc0e08877943b140b2ac019c6451670 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.

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