👉当前市面上的美容仪主要分三类:射频、微电流和LED光。射频美容仪主要通过射频和超声波技术促进胶原蛋白的产生,从而提升皮肤的紧致度,比如Tripollar Stop V就是这类代表;微电流美容仪主要通过微电流或者声波技术帮助皮肤紧致,促进护肤品吸收,NuFace是代表之一;LED光疗美容仪主要通过不同波长的光线来解决痘痘、色素沉淀和皱纹等皮肤问题,代表产品包括Neutorgena Light Therapy面罩和Currentbody系列LED美容仪。当然还有综合以上三种功能的,比如雅萌Max综合了以上所有,外加清洁和冷热技术,还有宙斯系列美容仪也是”十全大补“的产品。以上美容仪我几乎都有,但是现在全都在吃灰呢,除了Currentbody还在每天坚持用,因为它足够方便并且有效果。
👉我在2022年4月份买的Currentbody的面膜仪和颈纹仪套装,当时Dealmoon正好打折,我花了$462,前几天我看见Dealmoon的折扣又便宜了20多刀,可能是因为currentbody出新产品,开始清库存了,内地已经上市,估计北美也快了。
👉能让我坚持使用下来的原因
1、使用方便,每天只需要戴上10分钟就可以;
2、不用涂抹任何专用精华或者凝胶,洗完脸擦干就能用;
3、可携带式电池,充满一次电能用好久;
4、LED面罩美容仪的OG,据我所知,市面上很多类似的产品都是模仿它,何不直接入手这个鼻祖?
5、FDA权威认证,保证安全性和效果。
👉首先,什么是FDA?FDA(Food and Drug Administration)认证,是美国政府食品与药品管理总署签发的食品或药品的合格证书,由于其科学性和严谨性,这一认证已经成为世纪公认的标准。想要通过FDA认证非常困难,因为一旦获得FDA的药品,不仅可以在美国销售,而且可以在世界大多数国家销售。
👉Currentbody的LED面膜仪声称获得了FDA认证,如果真是这样,我们就可以放心大胆地使用它并且期待明显的效果了,但是奇怪的是,在FDA的官网http://www.fda.org我没查到它的认证,我已经发邮件给currentbody确认此事,正在等待他们的回复,然而我查到他们的另一款产品--Currentbody生发仪LED hair Regrowth确实在2023年4月5日获得了FDA认证。
👉使用心得:
我主要是想解决痘痘和痘印的问题,有效果。我以前用过Neutorgena Light Therapy面罩,原理跟这个类似,用完痘痘的确会瘪下去,但是那个activator是一次性的,一共可以用30次,用完要买新的,很烦很不环保。有了Currentbody这个面膜仪就可以一劳永逸了,颈纹仪让护肤没有死角,毕竟胸部以上都是脸。另外,用完之后肤色变得均匀了,毛孔变细腻了,但是没有发现有美白的功效。
❌缺点:
1、LED灯太亮晃眼睛,虽然官方保证绝对不会伤眼睛,但是每次用完,我都跟要瞎了一样,特别是闭眼睛的时候,光从眼睛缝里透进来,更亮。官方给出的解决方案是一个小黑眼罩,以前是附赠在面膜仪包装里,现在好像需要单独购买;
2、面罩鼻子那个位置,用完会留下红印,好一会才能消掉,所以不建议早上出门之前用;
3、面罩内部胶皮边缘时间久了会泛黄,有点影响观感。
👉结论:瑕不掩瑜,非常推荐!我已经安利了身边好几个小伙伴,反响都不错。
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官方回复如下:
Good Afternoon,
Thank you very much for your email.
Unfortunatley we can send that type of documentation out due to data protection, but we can confirm the Current body LED Mask is FDA-approved and made from medical-grade sillicone.
The mask also complies with the following medical certificates:
According to MDD 93/42/EEC, the CURRENTBODY Skin™ LED Light Therapy Mask is classified as a cosmetic device. However, for purposes of safety, we have conducted additional testing so that you can be assured of the safety and efficacy of the Cur-rentBody LED Mask.
The CurrentBody LED Mask has been tested to or complies with the following standards;EN 60601-1:2006/A12:2014.
Medical electrical equipment. General requirements for basic safety and essential performance.EN 60601-1-2:2015 Medical electrical equipment. General requirements for basic safety and essential performance. Collateral standard. Electromagnetic compatibility.
Requirements and tests.IEC 60601-1-6 2010 AMD12013 Medical Electrical Equipment – Part 1 General Requirements for Basic Safety and Essential Performance – Collateral Standard: Usability.IEC/EN60601-1-11:2015 Medical electrical equipment -- Part 1-11: General requirements for basic safety and essential performance -- Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment.IEC/EN 60601-2-57:2011
Medical electrical equipment. Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use.EN 62471:2008 Photobiological Safety of Lamps and Lamp Systems.EN 62366-1:2015 Application of usability engineering to medical devices, EN ISO 10993-1:2010-04 Biological evaluation of medical devices Part 1: Evaluation and testing.EN ISO 15223-1:2017
Medical Devices – Symbols to be used with medical device labels, labeling and information to be supplied – Part 1: General requirements.EN ISO 14.
EN ISO 14971:2012 Medical devices - Application of risk management to medical devices.
I have also provided the product manual for you to look over, I hope this information helps, please let me know if you have any further questions.
Kind regards,
Mickayla
Customer Care Team
CurrentBody
最新评论 5
:请问他们回复fda的问题了吗
:回复了,请看原文
:真的有用吗姐妹?
:有用,不过可以等等新款
回复 @房不胜房:好的,谢谢姐妹