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OPPO Arm Sling (Non-sterile) - Taiwan Registration ca0f238c50e136e7560ee9cec9cbc57b

Access comprehensive regulatory information for OPPO Arm Sling (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 ca0f238c50e136e7560ee9cec9cbc57b and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH 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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ca0f238c50e136e7560ee9cec9cbc57b
Registration Details
Taiwan FDA Registration: ca0f238c50e136e7560ee9cec9cbc57b
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Device Details

OPPO Arm Sling (Non-sterile)
TW: OPPOๆ‰‹่‡‚ๅŠๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ca0f238c50e136e7560ee9cec9cbc57b

Ministry of Health Medical Device Manufacturing Registration No. 004909

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the arm sling (O.3640) of the management measures for medical equipment.

o Equipment for physical medicine

O3640 arm sling

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024