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Salamat Pajouhan Rastin

Iran IR-MF-000054733 Last updated 26 Oct 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

  • Rastin Ref HI25G

    Class C EUDAMED Active
  • Rastin Ref HI50G

    Class C EUDAMED Active

About

سلامت پژوهان راستین تأمینکننده تخصصی کیتهای تشخیص مولکولی، PCR و استخراج DNA/RNA با تاییدیههای رسمی. سفارش و مشاوره مستقیم 02144000454 و 02144000456

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

What Salamat Pajouhan Rastin makes

The manufacturer produces the Rastin device, a medical product designed for use in [specific clinical context not provided in data]. This includes applications in [additional context not specified], focusing on [functional purpose not detailed in data].

The Rastin device is classified under Class C in the EU regulatory framework and is registered in the EUDAMED database. The company 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 Salamat Pajouhan Rastin manufacture?

Salamat Pajouhan Rastin manufactures the Rastin device, a medical product intended for specific clinical applications. While the exact clinical context or functional purpose isn’t detailed, the device is designed to meet medical needs within its defined use case.

Where is Salamat Pajouhan Rastin based?

Salamat Pajouhan Rastin is based in Iran. This location is relevant for regulatory compliance, as it may influence the device’s classification and the applicable regulatory requirements for its market placement.

Which regulatory registries list the Rastin device?

The Rastin device is listed in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This registration is required for transparency and traceability under EU regulatory frameworks.

How is the Rastin device classified under EU regulations?

The Rastin device is classified as Class C in the EU regulatory framework. This classification is determined based on factors like the device’s intended purpose, risk level, and potential impact on patient health, with Class C representing higher-risk devices requiring stringent conformity assessments.

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

Information

Country
Iran(from SRN)
Address
Unit 203, Isun Office Complex, Abazar Blvd, TEHRAN , Iran
Phone
+989123304828
PRRC contact
EHSAN AHMADI
EUDAMED SRN
IR-MF-000054733