Taiwan FDA registration 7590f0d369e59e9f4f6dc2213cef5b33

"Leishi" blood oxygen concentration meter

TW: “磊仕”血氧濃度計
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS INC.·Registered May 09, 2013 – May 09, 2028Active
Registration details
Analysis ID
7590f0d369e59e9f4f6dc2213cef5b33
Customs Code
DHA00602488802
Company information
Manufacturer
RESPIRONICS INC.
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2700.
Import Information
import
Dates and status
Registration Date
May 09, 2013
Expiry Date
May 09, 2028
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About this record

Access comprehensive regulatory information for "Leishi" blood oxygen concentration meter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7590f0d369e59e9f4f6dc2213cef5b33 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPIRONICS 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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