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"Medtronic" refill set - Taiwan Registration 6eaa34bcb28501cfdab9e0093e425d9b

Access comprehensive regulatory information for "Medtronic" refill set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eaa34bcb28501cfdab9e0093e425d9b and manufactured by MEDTRONIC NEUROMODULATION;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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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6eaa34bcb28501cfdab9e0093e425d9b
Registration Details
Taiwan FDA Registration: 6eaa34bcb28501cfdab9e0093e425d9b
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Device Details

"Medtronic" refill set
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅ†ๅ……ๅกซ็ต„ๅฅ—
Risk Class 2

Registration Details

6eaa34bcb28501cfdab9e0093e425d9b

DHA00601779705

Company Information

Product Details

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

J General hospital and personal use equipment

J.5965 Subcutaneous implantable intravascular injection port and guide

import

Dates and Status

Mar 12, 2007

Mar 12, 2027