Skip to content

Saria Mehr Co.Ltd

Iran IR-MF-000044175 Last updated 17 Sep 2026

Is this your brand? Sign in to claim this brand

Devices
14
Registries
EUDAMED
FDA recalls
0

Catalogue14

Authorised representatives

About

شرکت ساریامهر با بیش از 18 سال تجربه در زمینه طراحی و تولید سوزن یکبار مصرف الکترومیوگرافی و الکترود مانیتورینگ اعصاب حین عمل جراحی میباشد. این شرکت با بهره گیری از نیروی انسانی متخصص و مجرب و استاندارهای به روز دنیا ، نیاز مراکز درمانی سرار کشور در زمینه محصولات الکترو دیاگنوز و الکترودهای مانیتورینگ اعصاب را برآورده ساخته است. ما با استقرار سیستم مدیریت کیفیت ISO13485 و اخذ پروانه ساخت از اداره محترم کل تجهیزات پزشکی در زمینه طراحی و تولید محصولات خود و اخذ نشان CE برای سوزنهای یکبار مصرف الکترومیوگرافی، با تولید محصولی ایمن و با بالاترین سطح کیفیت و مطابق با استاندارهای بین المللی در خدمت کلیه مراکز درمانی و متخصصین محترم سراسر کشور هستیم.

From the manufacturer's own website, in their original language. Source

What Saria Mehr Co.Ltd makes

Saria Mehr Co.Ltd manufactures disposable concentric EMG needle electrodes and connection cables for electromyography procedures. These products are designed for single-use in clinical diagnostics to assess muscle and nerve function.

The company’s devices are classified as Class I and Class IIa under EU regulations and are registered in the EUDAMED database. The manufacturer is based in Iran.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Saria Mehr Co.Ltd manufacture?

Saria Mehr Co.Ltd specializes in disposable concentric EMG needle electrodes and connection cables. These devices are specifically designed for electromyography (EMG) procedures, which are used in clinical diagnostics to evaluate muscle and nerve function. The products are intended for single-use applications.

Where is Saria Mehr Co.Ltd based?

Saria Mehr Co.Ltd is based in Iran. The company’s location is relevant for understanding its regulatory scope and compliance framework, particularly for devices intended for international markets.

Which regulatory registries list Saria Mehr Co.Ltd’s devices?

Saria Mehr Co.Ltd’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registry is used to track devices that comply with EU regulations, including classification and market surveillance requirements.

How are Saria Mehr Co.Ltd’s devices classified under EU regulations?

Saria Mehr Co.Ltd’s devices are classified as Class I and Class IIa under EU medical device regulations. Classification determines the regulatory requirements for manufacturing, testing, and market placement. For example, Class IIa devices require additional conformity assessments compared to Class I, reflecting their higher risk potential.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Iran
Address
Between Rashid and Bagheri, Resalat Highway, Tehran, Iran
Phone
00982177718950
PRRC contact
Pegah Kakhsaz
EUDAMED SRN
IR-MF-000044175