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"Bruder" cold compress pack (unsterilized) - Taiwan Registration 8d3c211d7d7327329b0129964bb5f64d

Access comprehensive regulatory information for "Bruder" cold compress pack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d3c211d7d7327329b0129964bb5f64d and manufactured by BRUDER HEALTHCARE COMPANY. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.

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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8d3c211d7d7327329b0129964bb5f64d
Registration Details
Taiwan FDA Registration: 8d3c211d7d7327329b0129964bb5f64d
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Device Details

"Bruder" cold compress pack (unsterilized)
TW: โ€œๅธƒ้ญฏๅพทโ€ๅ†ทๆ•ทๅŒ… (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8d3c211d7d7327329b0129964bb5f64d

DHA04400538400

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

import

Dates and Status

Nov 28, 2006

Nov 28, 2011

Nov 08, 2012

Cancellation Information

Logged out

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