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"BIOTRONIK" Intracardiac defibrillator magnetic resonance imaging implantable active lead (including accessories) - Taiwan Registration 8f4f4cd369c398099a76f5f389492a65

Access comprehensive regulatory information for "BIOTRONIK" Intracardiac defibrillator magnetic resonance imaging implantable active lead (including accessories) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8f4f4cd369c398099a76f5f389492a65 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK 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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8f4f4cd369c398099a76f5f389492a65
Registration Details
Taiwan FDA Registration: 8f4f4cd369c398099a76f5f389492a65
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Device Details

"BIOTRONIK" Intracardiac defibrillator magnetic resonance imaging implantable active lead (including accessories)
TW: โ€œ็™พๅคšๅŠ›โ€ ไฟๅฟƒๅŠ›ๅฟƒๅ…ง้™ค้กซๅ™จ็ฃๆŒฏ้€ ๅฝฑๆคๅ…ฅๅผไธปๅ‹•ๅฐŽ็ทš(ๅŒ…ๆ‹ฌ้…ไปถ)
Risk Class 3

Registration Details

8f4f4cd369c398099a76f5f389492a65

DHA05603742206

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.3680 ๅฟƒ่ก€็ฎก็”จๆฐธไน…ๆˆ–ๆšซๆ™‚ๆ€งไน‹ๅฟƒๅพ‹่ชฟ็ฏ€ๅ™จ้›ปๆฅต

import

Dates and Status

Oct 02, 2024

Oct 02, 2029