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好文,这只新股可关注,谢谢!
@价值投资为王:贝康医疗:高瓴加持、基因检测行业迷你独角兽!
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2018-11-13
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贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 PGT是使用试剂制备植入前胚胎的DNA样本,然后由测序医疗器械读取并用于分析遗传病的成熟科学技术。 PGT一般可分为三种:非整倍体植入前基因检测(PGT-A)、单基因疾病植入前基因检测(PGT-M)和结构重排植入前基因检测(PGT-SR)。 PGT-A试剂盒用于在胚胎植入母体前检测试管婴儿过程中胚胎的非整倍体,即染色体数目异常。 该产品已获批准用于35岁或以上女性、此前经历三次或以上试管婴儿植入失败、曾自然流产或异常妊娠三次或以上、此前生育过染色体异常患儿的夫妇或存在染色体异常的夫妇。 根据弗若斯特沙利文的资料,贝康医疗的PGT-A试剂盒是唯一一个获国家药监局批准在中国进行商业销售的PGT试剂产品,而且潜在的国内外竞争对手的候选产品距离获得监管批准仍有数年之遥。 在市场空间上,由于贝康医疗于2020年才成功首家推出PGT-A试剂盒,预期市场规模(按基于出厂价的销售收入计)从2020年的人民币95.9百万元增加至2025年的人民币3","listText":"贝康医疗是一家辅助生殖基因检测创新公司,旗下产品PGT-A试剂盒是首个也是唯一已获国家药监局批准的三代试管婴儿基因检测试剂盒。 贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 PGT是使用试剂制备植入前胚胎的DNA样本,然后由测序医疗器械读取并用于分析遗传病的成熟科学技术。 PGT一般可分为三种:非整倍体植入前基因检测(PGT-A)、单基因疾病植入前基因检测(PGT-M)和结构重排植入前基因检测(PGT-SR)。 PGT-A试剂盒用于在胚胎植入母体前检测试管婴儿过程中胚胎的非整倍体,即染色体数目异常。 该产品已获批准用于35岁或以上女性、此前经历三次或以上试管婴儿植入失败、曾自然流产或异常妊娠三次或以上、此前生育过染色体异常患儿的夫妇或存在染色体异常的夫妇。 根据弗若斯特沙利文的资料,贝康医疗的PGT-A试剂盒是唯一一个获国家药监局批准在中国进行商业销售的PGT试剂产品,而且潜在的国内外竞争对手的候选产品距离获得监管批准仍有数年之遥。 在市场空间上,由于贝康医疗于2020年才成功首家推出PGT-A试剂盒,预期市场规模(按基于出厂价的销售收入计)从2020年的人民币95.9百万元增加至2025年的人民币3","text":"贝康医疗是一家辅助生殖基因检测创新公司,旗下产品PGT-A试剂盒是首个也是唯一已获国家药监局批准的三代试管婴儿基因检测试剂盒。 贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 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贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 PGT是使用试剂制备植入前胚胎的DNA样本,然后由测序医疗器械读取并用于分析遗传病的成熟科学技术。 PGT一般可分为三种:非整倍体植入前基因检测(PGT-A)、单基因疾病植入前基因检测(PGT-M)和结构重排植入前基因检测(PGT-SR)。 PGT-A试剂盒用于在胚胎植入母体前检测试管婴儿过程中胚胎的非整倍体,即染色体数目异常。 该产品已获批准用于35岁或以上女性、此前经历三次或以上试管婴儿植入失败、曾自然流产或异常妊娠三次或以上、此前生育过染色体异常患儿的夫妇或存在染色体异常的夫妇。 根据弗若斯特沙利文的资料,贝康医疗的PGT-A试剂盒是唯一一个获国家药监局批准在中国进行商业销售的PGT试剂产品,而且潜在的国内外竞争对手的候选产品距离获得监管批准仍有数年之遥。 在市场空间上,由于贝康医疗于2020年才成功首家推出PGT-A试剂盒,预期市场规模(按基于出厂价的销售收入计)从2020年的人民币95.9百万元增加至2025年的人民币3","listText":"贝康医疗是一家辅助生殖基因检测创新公司,旗下产品PGT-A试剂盒是首个也是唯一已获国家药监局批准的三代试管婴儿基因检测试剂盒。 贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 PGT是使用试剂制备植入前胚胎的DNA样本,然后由测序医疗器械读取并用于分析遗传病的成熟科学技术。 PGT一般可分为三种:非整倍体植入前基因检测(PGT-A)、单基因疾病植入前基因检测(PGT-M)和结构重排植入前基因检测(PGT-SR)。 PGT-A试剂盒用于在胚胎植入母体前检测试管婴儿过程中胚胎的非整倍体,即染色体数目异常。 该产品已获批准用于35岁或以上女性、此前经历三次或以上试管婴儿植入失败、曾自然流产或异常妊娠三次或以上、此前生育过染色体异常患儿的夫妇或存在染色体异常的夫妇。 根据弗若斯特沙利文的资料,贝康医疗的PGT-A试剂盒是唯一一个获国家药监局批准在中国进行商业销售的PGT试剂产品,而且潜在的国内外竞争对手的候选产品距离获得监管批准仍有数年之遥。 在市场空间上,由于贝康医疗于2020年才成功首家推出PGT-A试剂盒,预期市场规模(按基于出厂价的销售收入计)从2020年的人民币95.9百万元增加至2025年的人民币3","text":"贝康医疗是一家辅助生殖基因检测创新公司,旗下产品PGT-A试剂盒是首个也是唯一已获国家药监局批准的三代试管婴儿基因检测试剂盒。 贝康医疗2014年开始开发PGT-A试剂盒,于2020年2月拿到国家药监局三类医疗器械注册证。 三类医疗器械指的是用于植入人体或支持维持生命,对人体具有潜在危险,对其安全性、有效性必须严格控制的医疗器械。如植入式心脏起搏器、人工心脏瓣膜等; 二类医疗器械指的是为对其安全性、有效性应当加以控制的医疗器械。如体温计、血压计、内窥镜等。 由此可见,贝康医疗的PGT-A试剂盒有较高的含科量,加上独一无二的地位,贝康吸引了高瓴资本在内的明星机构入场。 对于贝康医疗,整体的感受就是一家基因检测行业迷你独角兽,分析医疗股,同样要从产品竞争力、市场空间及竞争格局入手,接下来,本文逐一对贝康医疗的产品进行分析。 独一无二PGT-A试剂盒 PGT是使用试剂制备植入前胚胎的DNA样本,然后由测序医疗器械读取并用于分析遗传病的成熟科学技术。 PGT一般可分为三种:非整倍体植入前基因检测(PGT-A)、单基因疾病植入前基因检测(PGT-M)和结构重排植入前基因检测(PGT-SR)。 PGT-A试剂盒用于在胚胎植入母体前检测试管婴儿过程中胚胎的非整倍体,即染色体数目异常。 该产品已获批准用于35岁或以上女性、此前经历三次或以上试管婴儿植入失败、曾自然流产或异常妊娠三次或以上、此前生育过染色体异常患儿的夫妇或存在染色体异常的夫妇。 根据弗若斯特沙利文的资料,贝康医疗的PGT-A试剂盒是唯一一个获国家药监局批准在中国进行商业销售的PGT试剂产品,而且潜在的国内外竞争对手的候选产品距离获得监管批准仍有数年之遥。 在市场空间上,由于贝康医疗于2020年才成功首家推出PGT-A试剂盒,预期市场规模(按基于出厂价的销售收入计)从2020年的人民币95.9百万元增加至2025年的人民币3","images":[{"img":"https://static.tigerbbs.com/1cd69ac55c471b36a727fda085dafb34","width":"1256","height":"598"},{"img":"https://static.tigerbbs.com/a30b90dc63007e288af69f8740b6f927","width":"932","height":"361"},{"img":"https://static.tigerbbs.com/4d9e33e6acc6793b3a649cebb18daa51","width":"1075","height":"670"}],"top":1,"highlighted":2,"essential":2,"paper":2,"likeSize":0,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/310818111","isVote":1,"tweetType":1,"viewCount":0,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":7,"langContent":"CN","totalScore":0},"isVote":1,"tweetType":1,"viewCount":993,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"CN","totalScore":0},{"id":329729,"gmtCreate":1542122286804,"gmtModify":1704780680645,"author":{"id":"3496794574457837","authorId":"3496794574457837","name":"御浪前行","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":4,"crmLevelSwitch":0,"followedFlag":false},"themes":[],"htmlText":"这篇文章不错,转发给大家看","listText":"这篇文章不错,转发给大家看","text":"这篇文章不错,转发给大家看","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":0,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/329729","repostId":"329361","repostType":1,"isVote":1,"tweetType":1,"viewCount":1510,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"CN","totalScore":0}],"lives":[]}