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"ME" Arm Splint (NON-STERILE) - Taiwan Registration 6307c9b50221bfc1c94e1edd8dd51af6

Access comprehensive regulatory information for "ME" Arm Splint (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6307c9b50221bfc1c94e1edd8dd51af6 and manufactured by Mingyi Disability Rehabilitation Equipment Co., Ltd. The authorized representative in Taiwan is Mingyi Disability Rehabilitation Equipment 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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6307c9b50221bfc1c94e1edd8dd51af6
Registration Details
Taiwan FDA Registration: 6307c9b50221bfc1c94e1edd8dd51af6
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Device Details

"ME" Arm Splint (NON-STERILE)
TW: "ๆ˜Žๆ†ถ"ๆ‰‹่…ณๅ›บๅฎšๅธถ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6307c9b50221bfc1c94e1edd8dd51af6

Ministry of Health Medical Device Manufacturing Registration No. 001329

Company Information

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2026