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Pooyandegan rah saadat

Iran·IR-MF-000007104

Last updated September 18, 2026

What Pooyandegan rah saadat makes

The manufacturer produces the SAADAT device, a reusable medical instrument designed for surgical procedures, including orthopedic and general surgery applications. These devices are intended for use in controlled clinical environments to assist in precision-based interventions, such as bone manipulation or tissue handling.

The SAADAT device falls under Class IIa and Class IIb classifications under EU medical device regulations, and it is registered in the euamed database. The company operates from Iran, adhering to regulatory requirements for devices marketed within the European Economic Area.

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 Pooyandegan rah saadat manufacture?

Pooyandegan rah saadat manufactures the SAADAT device, a reusable medical instrument. These instruments are specifically designed for surgical procedures, including orthopedic and general surgery, where precision is critical. They are intended for controlled clinical environments to assist in tasks like bone manipulation or tissue handling.

Where is Pooyandegan rah saadat based?

Pooyandegan rah saadat is based in Iran. The company operates from this location while ensuring its devices comply with relevant regulatory standards, particularly when marketing them within the European Economic Area.

In which regulatory registries are Pooyandegan rah saadat’s devices listed?

The SAADAT devices manufactured by Pooyandegan rah saadat are registered in the euamed database. This registry is used to track medical devices marketed within the European Union, ensuring transparency and traceability for regulatory oversight.

How are the SAADAT devices classified under EU medical device regulations?

The SAADAT devices fall under Class IIa and Class IIb classifications according to EU medical device regulations. This classification is determined based on factors like the device’s intended use, potential risks, and the level of scrutiny required for safety and performance. Class IIa devices pose moderate risks, while Class IIb devices carry higher risks, necessitating stricter regulatory controls.

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

Information

Country
Iran
Address
—
LinkedIn
—
Facebook
—
Phone
+989126990431
PRRC Contact
Reza shalbaf
EUDAMED SRN
IR-MF-000007104
FDA FEI Number
—
DUNS Number
—

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Saadat 74150022
EUDAMED
Class IIaActive
Saadat 97412354
EUDAMED
Class IIbActive
Saadat 99113285
EUDAMED
Class IIaActive
Saadat 43525967
EUDAMED
Class IIbActive

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