Taiwan FDA registration f0cae26f3b99d8c5d0986ab1edf1e50b

"Lei" multiple sleep physiological recorder

TW: “磊士”多重睡眠生理紀錄儀
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS INC.·Registered Mar 03, 2010 – Mar 03, 2030Active
Registration details
Analysis ID
f0cae26f3b99d8c5d0986ab1edf1e50b
Customs Code
DHA00602062206
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)
K Neuroscience
Product Type (Level 2)
K.1400 Brain Wave Scanner
Import Information
import
Dates and status
Registration Date
Mar 03, 2010
Expiry Date
Mar 03, 2030
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About this record

Access comprehensive regulatory information for "Lei" multiple sleep physiological recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0cae26f3b99d8c5d0986ab1edf1e50b 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 2 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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