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“Cochlear” Nucleus Sound Processors & Accessories - Taiwan Registration bd85907d5b10d1b2c1fa94ec14907095

Access comprehensive regulatory information for “Cochlear” Nucleus Sound Processors & Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bd85907d5b10d1b2c1fa94ec14907095 and manufactured by COCHLEAR LIMITED. The authorized representative in Taiwan is Cochlear Taiwan Limited.

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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bd85907d5b10d1b2c1fa94ec14907095
Registration Details
Taiwan FDA Registration: bd85907d5b10d1b2c1fa94ec14907095
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Device Details

“Cochlear” Nucleus Sound Processors & Accessories
TW: "科利耳" 人工耳蝸聲音處理器及附件
Risk Class 3
MD

Registration Details

bd85907d5b10d1b2c1fa94ec14907095

Ministry of Health Medical Device Import No. 026766

DHA05602676601

Company Information

Australia

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT device

G0001 Cochlear implant

Imported from abroad

Dates and Status

Oct 28, 2014

Oct 28, 2024