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氧舱知识答疑
微高压氧舱是否有 3C 认证、医疗器械相关合规证书?
Date: 2026-10-31
微高压氧舱属于民用微高压氧舱不属于二类 / 三类医疗器械,不需要医疗器械注册证。
氧舱主机的空压机、电控系统等整机做安全测试。很多采购客户容易混淆医用高压氧舱与民用微高压氧舱,医用款才需要医疗器械注册证,商用康养微高压氧舱执行民用产品相关国标。
洛邦尚品微高压氧舱拥有 CE、RoHS、GB 相关检测报告,可向采购方出示证书原件扫描件,方便企业采购前期合规审核。
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民用微高压氧舱需要报备备案吗?不备案会不会被监管查处?
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企业采购微高压氧舱需要哪些正规资质和检测报告?
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Household micro hyperbaric oxygen chamber
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Micro hyperbaric oxygen chamber in healthcare facilities
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