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Sonoma Pharmaceuticals Successfully Transitions First Products to New EU MDR Requirements for Class IIb Medical Devices

Sonoma Pharmaceuticals Successfully Transitions First Products to New EU MDR Requirements for Class IIb Medical Devices

sonoma pharmaceuticals 成功将首批产品过渡到新的欧盟医疗设备监管要求下的 IIb 类医疗设备
Accesswire ·  12/05 21:30

BOULDER, CO / ACCESSWIRE / December 5, 2024 / Sonoma Pharmaceuticals, Inc. (Nasdaq:SNOA), a global healthcare leader developing and producing patented Microcyn technology based stabilized hypochlorous acid (HOCl) products for a wide range of applications, including wound care, eye, oral and nasal care, dermatological conditions, podiatry, and animal health care, today announced it has successfully completed transition to the new European Union (EU) Medical Device Regulation (MDR) for four of its products in Europe.

科罗拉多州博尔德 / ACCESSWIRE / 2024年12月5日 / sonoma pharmaceuticals, Inc. (纳斯达克:SNOA),一家全球医疗保健领导者,开发并生产专利的Microcyn技术基础的稳定次氯酸(HOCl)产品,适用于广泛的应用领域,包括伤口护理、眼部、口腔和鼻部护理、皮肤病、足病以及动物医疗保健,今天宣布已成功完成四款产品在欧洲的新欧盟医疗设备条例(MDR)的转换。

Sonoma was granted classification as a Class IIb medical device for Microdacyn60 Wound Care and Microdacyn60 Hydrogel, its scar gel product Epicyn, and Pediacyn for atopic dermatitis.

sonoma被授予Microdacyn60伤口护理和Microdacyn60水凝胶、其疤痕胶产品Epicyn以及用于特应性皮炎的Pediacyn作为IIb类医疗设备的分类。

The MDR was adopted in the EU in 2017 to replace the existing Medical Device Directive. The transition period for compliance was most recently extended to December 31, 2028 for non-implantable Class IIb and lower risk devices. In order to comply with the MDR, Sonoma's products needed to meet certain requirements relating to safety and performance and successfully undergo verification of regulatory compliance, or conformity assessment.

MDR于2017年在欧盟通过,以取代现有的医疗设备指令。合规的过渡期最近延长至2028年12月31日,适用于非植入式IIb类及更低风险设备。为了遵循MDR,sonoma的产品需要满足与安全性和性能相关的特定要求,并成功通过监管合规性验证或符合性评估。

"Sonoma is pleased to have received the new Class IIb classification for our wound care, scar and atopic dermatitis products in the European Union, well ahead of the requisite compliance deadline," said Amy Trombly, CEO of Sonoma. "It is truly a testimony to the safety and efficacy of our products and strength of our clinical data. This is an important milestone made possible by the diligent preparation of our regulatory team to meet these new and more stringent standards for medical devices in Europe."

“sonoma很高兴能在欧洲联盟获得我们伤口护理、疤痕和特应性皮炎产品的新IIb类分类,远远早于必要的合规截止日期,”sonoma首席执行官艾米·特罗布利(Amy Trombly)说。“这确实证明了我们产品的安全性和有效性以及我们临床数据的力量。这是一个重要的里程碑,得益于我们的监管团队的认真准备,使我们能够满足欧洲医疗设备的新和更严格的标准。”

About Sonoma Pharmaceuticals, Inc.

关于Sonoma Pharmaceuticals, Inc.

Sonoma Pharmaceuticals is a global healthcare leader for developing and producing stabilized hypochlorous acid (HOCl) products for a wide range of applications, including wound, eye, oral and nasal care, dermatological conditions, podiatry, animal health care and non-toxic disinfectants. Sonoma's products are clinically proven to reduce itch, pain, scarring, and irritation safely and without damaging healthy tissue. In-vitro and clinical studies of HOCl show it to safely manage skin abrasions, lacerations, minor irritations, cuts, and intact skin. Sonoma's products are sold either directly or via partners in 55 countries worldwide and the company actively seeks new distribution partners. The company's principal office is in Boulder, Colorado, with manufacturing operations in Guadalajara, Mexico. European marketing and sales are headquartered in Roermond, Netherlands. More information can be found at . For partnership opportunities, please contact busdev@sonomapharma.com.

Sonoma Pharmaceuticals是一家全球医疗保健领导者,为广泛的应用领域(包括伤口护理、眼科、口腔和鼻部护理、皮肤病状、足病和动物保健等)开发和生产稳定的次氯酸(HOCl)产品和无毒消毒剂。Sonoma的产品经临床证明能够安全地减轻瘙痒、疼痛、瘢痕和刺激,而不会损伤健康组织。HOCl的体外和临床研究表明,它能够安全地管理皮肤破损、撕裂、轻微刺激、切口以及完好的皮肤。Sonoma的产品在全球55个国家直接销售或通过伙伴销售,公司同时寻求新的分销伙伴。公司总部设在科罗拉多的博尔德市,制造业务位于墨西哥瓜达拉哈拉,欧洲营销和销售业务总部设在荷兰罗尔蒙德。可以在sonomapharma.com获得更多信息。如有合作机会,请联系busdev@sonomapharma.com。

Forward-Looking Statements

前瞻性声明

Except for historical information herein, matters set forth in this press release are forward-looking within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, including statements about the commercial and technology progress and future financial performance of Sonoma Pharmaceuticals, Inc. and its subsidiaries (the "company"). These forward-looking statements are identified by the use of words such as "continue," "develop," "anticipate," "expect" and "expand," among others. Forward-looking statements in this press release are subject to certain risks and uncertainties inherent in the company's business that could cause actual results to vary, including such risks that regulatory clinical and guideline developments may change, scientific data may not be sufficient to meet regulatory standards or receipt of required regulatory clearances or approvals, clinical results may not be replicated in actual patient settings, protection offered by the company's patents and patent applications may be challenged, invalidated or circumvented by its competitors, the available market for the company's products will not be as large as expected, the company's products will not be able to penetrate one or more targeted markets, revenues will not be sufficient to meet the company's cash needs, fund further development, and the ability to meet a multitude of diverse regulatory and marketing requirements in different countries and municipalities, and other risks detailed from time to time in the company's filings with the Securities and Exchange Commission. The company disclaims any obligation to update these forward-looking statements, except as required by law.

除了此处的历史信息之外,本新闻稿中所述事项均为1995年《私人证券诉讼改革法案》中“安全港”条款下的前瞻性声明,包括关于sonoma pharmaceuticals公司的商业和科技进展以及未来财务表现的陈述。这些前瞻性声明通过使用“继续”、“发展”、“预期”、“期待”和“扩展”等词语来识别。本新闻稿中的前瞻性声明受到公司业务固有的某些风险和不确定性的影响,这些风险可能导致实际结果有所不同,包括:监管临床和指导方针的发展可能会发生变化,科学数据可能不足以达到监管标准或获得所需的监管批准,临床结果可能无法在实际患者环境中复制,公司专利和专利申请提供的保护可能会受到竞争对手的挑战、被裁定无效或绕过,公司产品的可用市场可能不会像预期的那样庞大,公司产品可能无法进入一个或多个目标市场,收入可能不足以满足公司的现金需求,无法进一步发展,以及在不同国家和城市满足多种多样的监管和市场要求的能力,以及在公司定期向证券交易委员会提交的文件中详细说明的其他风险。除法律要求外,公司不承担更新这些前瞻性声明的义务。

Sonoma Pharmaceuticals, Microcyn60, Epicyn and Pediacyn are trademarks or registered trademarks of Sonoma Pharmaceuticals, Inc. All other trademarks and service marks are the property of their respective owners.

sonoma pharmaceuticals、Microcyn60、Epicyn和Pediacyn是sonoma pharmaceuticals公司的商标或注册商标。所有其他商标和服务标志均为各自所有者的财产。

Media and Investor Contact:

媒体和投资者联系方式:

Sonoma Pharmaceuticals, Inc.
ir@sonomapharma.com

Sonoma Pharmaceuticals,Inc。
ir@sonomapharma.com

SOURCE: Sonoma Pharmaceuticals, Inc.

来源:Sonoma Pharmaceuticals,Inc。


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