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"Kangenfei" powered treatment unit (non-sterilized) - Taiwan Registration ef657c91ef6233593423e4cf2c674e64

Access comprehensive regulatory information for "Kangenfei" powered treatment unit (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef657c91ef6233593423e4cf2c674e64 and manufactured by HUANGSHAN JINFU MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is RUI-HUNG INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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ef657c91ef6233593423e4cf2c674e64
Registration Details
Taiwan FDA Registration: ef657c91ef6233593423e4cf2c674e64
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Device Details

"Kangenfei" powered treatment unit (non-sterilized)
TW: "ๅบทๆฉ่ฒ" ๅ‹•ๅŠ›ๅผๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ef657c91ef6233593423e4cf2c674e64

DHA09600501004

Company Information

Product Details

Limited to the first level of identification scope of the "Power Treatment Table (O.3760)" of the Measures for the Classification and Grading of Medical Devices.

o Physical Medical Sciences

O.3760 Powered therapy cage

QMS/QSD;; Input;; Chinese goods

Dates and Status

Oct 21, 2024

Oct 21, 2029