1
关注
1136
浏览

the interests in the review of metallicpowder materials for additive?

您还未登录!暂时最多只可查看 1 条回答

登录! 还没有账号?去注册

si4520 一阶会员 用户来自于: 广东省深圳市
2023-09-18 20:50

The technical review of metallic powder materials foradditive manufacturing in dentistry mainly focus on three aspects:the performance requirements of metallic powder for additivemanufacturing in dentistry, the process parameter validation ofadditive manufacturing and the performance of printed test piecesafter additive manufacturing and forming.The performancerequirements of metallic powder for additive manufacturing indentistry include but not limited chemical composition (oxygen,hydrogen and impurity elements), sphericity, powder particle sizeand size distribution, fiowability, apparent density, and tap densityFor process parameter validation of additive manufacturing, it is necessary to clarify the printing parameters of the printing equipmentand printing equipment systems compatible with the productincluding but not limited to laser power, spot diameter, scanninginterval, powder spreading thickness and scanning speed. In additionit is necessary to submit the validation and verification report onvarious parameters and specify the relevant parameters in producttechnical requirements (PTR) and instructions for use (IFU).Theperformance requirements for the printed test piece after additivemanufacturing and forming include the verification of the mechanicalstrength of the printed test piece in each direction, which shouldsimulate as far as possible the actual use of the dental restorationsin clinical application, with its fatigue and resistance to repeatedbending taken into consideration. The corrosion resistance, inclusionsand porosity, and warping of the printed test piece should also beverified.


关于作者

问题动态

发布时间
2023-09-18 20:50
更新时间
2023-09-18 20:50
关注人数
1 人关注

推荐内容

临床试验后再补充检验,是否合规?
有源产品变更增加型号,是否必须进行检测?
首次注册产品,能否在不同的检验所分别检测EMC和安规?
设计多项标志物联合检测产品需要考虑的问题有哪些?如何确定多项联检试剂的不同组合形式是否可以作为同一注册单元?
体外诊断试剂自测产品注册时说明书可以注册两个版本么,即一个用于专业医疗机构人员使用,一个用于非专业背景的人员自测使用?
产品名称变更,是变更注册还是变更备案,是否可以快审?
高分子材料为原材料的疝气修复补片,洁净生产环境要求是什么?
一次性防护服新增大尺寸的型号规格产品,注册检测时可以只检测新增型号的尺寸要求?变更材料中,是否可以提供有效期、包装、运输验证的评价报告,豁免相关实验?
定量检测体外诊断试剂的精密度试验设计,是否要对各影响因素进行单独评估?
企业参考品相关信息是否要写入技术要求?