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Fibli Kaixun Rehabilitation Equipment and Accessories (Unsterilized) - Taiwan Registration 67d6bec5b55ac36b507684dbc910a2b0

Access comprehensive regulatory information for Fibli Kaixun Rehabilitation Equipment and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67d6bec5b55ac36b507684dbc910a2b0 and manufactured by FABRICATION ENTERPRISES INCORPORATED. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

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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67d6bec5b55ac36b507684dbc910a2b0
Registration Details
Taiwan FDA Registration: 67d6bec5b55ac36b507684dbc910a2b0
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Device Details

Fibli Kaixun Rehabilitation Equipment and Accessories (Unsterilized)
TW: "่ฒๅธƒๅˆฉๅ‡ฑ่จŠ"ๅพฉๅฅ็”จ่ฃๅ…ทๅŠ้…ไปถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

67d6bec5b55ac36b507684dbc910a2b0

DHA04401257801

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment classification and grading management measures for prosthetics and accessories for accessories (O.3025).

o Physical Medical Sciences

O.3025 ็พฉ่‚ขๅŠ่ฃๅ…ท็”จ้™„ไปถ

import

Dates and Status

Jan 10, 2013

Jan 10, 2028