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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 成功將首批產品過渡到新的歐盟醫療設備監管要求下的 IIb 類醫療設備
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.

科羅拉多州博爾德/ACCESSWIRE/2024年12月5日/索諾瑪製藥公司(納斯達克股票代碼:SNOA)是一家全球醫療保健領導者,開發和生產基於Microcyn技術的專利穩定次氯酸(HOCl)產品,其應用範圍廣泛,包括傷口護理、眼部、口腔和鼻腔護理、皮膚病、足病和動物保健,今天宣佈已成功完成向新歐洲的過渡歐盟(歐盟)醫療器械法規(MDR)適用於其在歐洲的四種產品。

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.

索諾瑪被評爲Microdacyn60傷口護理和Microdacyn60水凝膠、其疤痕凝膠產品Epicyn和治療特應性皮炎的Pediacyn的IIb類醫療器械。

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.

歐盟於2017年通過了MDR,以取代現有的醫療器械指令。非植入式IIb類和低風險設備的合規過渡期最近延長至2028年12月31日。爲了符合 MDR,索諾瑪的產品需要滿足與安全和性能相關的某些要求,併成功通過監管合規性驗證或合規性評估。

"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."

索諾瑪首席執行官艾米·特隆布利表示:「索諾瑪很高興我們在歐盟的傷口護理、疤痕和特應性皮炎產品在必要的合規截止日期之前獲得了新的IIb類分類。」「這確實證明了我們產品的安全性和有效性以及我們臨床數據的力量。這是一個重要的里程碑,這要歸功於我們的監管團隊爲滿足歐洲這些新的、更嚴格的醫療器械標準所做的辛勤準備。」

About Sonoma Pharmaceuticals, Inc.

關於索諾瑪製藥公司

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.

索諾瑪製藥是全球醫療保健領導者,開發和生產穩定的次氯酸(HOCl)產品,其應用範圍廣泛,包括傷口、眼睛、口腔和鼻腔護理、皮膚病、足病學、動物保健和無毒消毒劑。經臨床證明,索諾瑪的產品可以安全地減輕瘙癢、疼痛、疤痕和刺激,不會損壞健康組織。HOCl 的體外和臨床研究表明,它可以安全地管理皮膚擦傷、割傷、輕微刺激、割傷和皮膚完好無損。索諾瑪的產品直接或通過合作伙伴在全球55個國家銷售,該公司積極尋找新的分銷合作伙伴。該公司的總部位於科羅拉多州的博爾德,製造業務位於墨西哥瓜達拉哈拉。歐洲的營銷和銷售總部位於荷蘭魯爾蒙德。更多信息可以在以下網址找到。如需合作機會,請聯繫 busdev@sonomapharma.com。

Forward-Looking Statements

前瞻性陳述

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.

除此處的歷史信息外,根據1995年《私人證券訴訟改革法》的 「安全港」 條款,包括有關索諾瑪製藥公司及其子公司(「公司」)商業和技術進步以及未來財務業績的聲明,本新聞稿中列出的事項均具有前瞻性。這些前瞻性陳述是通過使用 「繼續」、「發展」、「預測」、「期望」 和 「擴大」 等詞語來識別的。本新聞稿中的前瞻性陳述受公司業務固有的某些風險和不確定性的影響,這些風險和不確定性可能導致實際業績發生變化,包括監管臨床和指南的制定可能發生變化、科學數據可能不足以滿足監管標準或無法獲得所需的監管許可或批准、臨床結果可能無法在實際患者環境中複製、公司專利和專利申請提供的保護可能會受到質疑、失效或規避以下風險:其競爭對手,公司產品的可用市場將不如預期的那麼大,公司的產品將無法滲透到一個或多個目標市場,收入將不足以滿足公司的現金需求、爲進一步發展提供資金、滿足不同國家和城市多種不同的監管和營銷要求的能力,以及公司向證券交易委員會提交的文件中不時詳述的其他風險。除非法律要求,否則公司不承擔任何更新這些前瞻性陳述的義務。

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.

索諾瑪製藥、Microcyn60、Epicyn和Pediacyn是索諾瑪製藥公司的商標或註冊商標。所有其他商標和服務標誌均爲其各自所有者的財產。

Media and Investor Contact:

媒體和投資者聯繫人:

Sonoma Pharmaceuticals, Inc.
ir@sonomapharma.com

索諾瑪製藥有限公司
ir@sonomapharma.com

SOURCE: Sonoma Pharmaceuticals, Inc.

來源:索諾瑪製藥公司


譯文內容由第三人軟體翻譯。


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