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Johnson & Johnson in vitro prosthetic components (unsterilized)  - Taiwan Registration 05c2a959266979c82e14fc978e6e9bc7

Access comprehensive regulatory information for Johnson & Johnson in vitro prosthetic components (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 05c2a959266979c82e14fc978e6e9bc7 and manufactured by OHIO WILLOW WOOD COMPANY. The authorized representative in Taiwan is JOHNSON A. L. TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JOHNSON PROSTHETIC & ORTHOTIC LABORATORIES INCORPORATION, and 1 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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05c2a959266979c82e14fc978e6e9bc7
Registration Details
Taiwan FDA Registration: 05c2a959266979c82e14fc978e6e9bc7
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Device Details

Johnson & Johnson in vitro prosthetic components (unsterilized) 
TW: “強生”體外肢體義肢用組件 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

05c2a959266979c82e14fc978e6e9bc7

DHA04400959007

Company Information

United States

Product Details

Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.

o Physical Medical Sciences

O.3420 體外肢體義肢用組件

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Dates and Status

Nov 26, 2010

Nov 26, 2025

Sep 30, 2021

Cancellation Information

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