"Holly" polyetheretherketone lumbar intervertebral fusion - Taiwan Registration e2e8c46efe3d4f83f8cf005baf0dfa1d
Access comprehensive regulatory information for "Holly" polyetheretherketone lumbar intervertebral fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2e8c46efe3d4f83f8cf005baf0dfa1d and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER CO., LTD..
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e2e8c46efe3d4f83f8cf005baf0dfa1d
Registration Details
Taiwan FDA Registration: e2e8c46efe3d4f83f8cf005baf0dfa1d
Device Details
"Holly" polyetheretherketone lumbar intervertebral fusion
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Risk Class 2

