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OsteoSelect PLUS DBM Putty - Taiwan Registration 778bad1a84e7fff45b06e96e3fb1d5fb

Access comprehensive regulatory information for OsteoSelect PLUS DBM Putty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 778bad1a84e7fff45b06e96e3fb1d5fb and manufactured by Xtant Medical Holdings, Inc.. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL 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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778bad1a84e7fff45b06e96e3fb1d5fb
Registration Details
Taiwan FDA Registration: 778bad1a84e7fff45b06e96e3fb1d5fb
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Device Details

OsteoSelect PLUS DBM Putty
TW: ๆญ็‰น้ธๅŠ ๅŽป็คฆๅŒ–่ฃœ้ชจ็‰ฉ
Risk Class 2
MD

Registration Details

778bad1a84e7fff45b06e96e3fb1d5fb

Ministry of Health Medical Device Import No. 031355

DHA05603135500

Company Information

United States

Product Details

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

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Jul 23, 2018

Jul 23, 2028