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"Medtronic" Crison vertebral body filler - Taiwan Registration b8059fb5909289a080a19f502c00ed12

Access comprehensive regulatory information for "Medtronic" Crison vertebral body filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b8059fb5909289a080a19f502c00ed12 and manufactured by MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO, and 1 recent registrations in the same category. 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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b8059fb5909289a080a19f502c00ed12
Registration Details
Taiwan FDA Registration: b8059fb5909289a080a19f502c00ed12
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Device Details

"Medtronic" Crison vertebral body filler
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅ…‹้‡ŒๆฃฎๆคŽ้ซ”ๅกซๅ……ๅ™จ
Risk Class 2
Cancelled

Registration Details

b8059fb5909289a080a19f502c00ed12

DHA00601845702

Company Information

Product Details

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

N Orthopedics

import

Dates and Status

Nov 23, 2007

Nov 23, 2012

Mar 29, 2013

Cancellation Information

Logged out

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