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"Ofah" Acus limb equipment (unsterilized) - Taiwan Registration dca5088800a760ac05cfbe887efb275e

Access comprehensive regulatory information for "Ofah" Acus limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dca5088800a760ac05cfbe887efb275e and manufactured by OFA BAMBERG GMBH. The authorized representative in Taiwan is MEDIBIOT 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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dca5088800a760ac05cfbe887efb275e
Registration Details
Taiwan FDA Registration: dca5088800a760ac05cfbe887efb275e
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Device Details

"Ofah" Acus limb equipment (unsterilized)
TW: โ€œๆญๆณ•โ€้˜ฟๅบซๆ–ฏ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dca5088800a760ac05cfbe887efb275e

DHA04400711608

Company Information

Germany

Product Details

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

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

Oct 14, 2008

Oct 14, 2023

Sep 30, 2021

Cancellation Information

Logged out

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