Sina Hamd Aria
Iran IR-MF-000025622 Last updated 21 Oct 2026
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- Devices
- 21
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Sina Ref 9006010059
Sina Ref 9009020596
Sina Ref 9007010128
Sina Ref 9023000008
Sina Ref 1509000413
Sina Ref 9003000051
Sina Ref 9001010318
Sina Ref 9005010001
Sina Ref 9005010200
Sina Ref 9022000005
Sina Ref 9005010078
Sina Ref 9010000020
Sina Ref 9002010387
Sina Ref 9009020442
Sina Ref 9005010199
Sina Ref 9001010416
Sina Ref 9002010376
sina radiant warmer Ref WI 0717-WI 0718
Sina Ref 9005010166
Sina Ref 9002020518
Sina Ref 9005010100
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About
ما برآنیم که در سینا, همگام با تکنولوژی روز دنیا در R&D و تولید و بهره گیری از نیروی متخصص جوان کشور و همچنین مشاوران زبده و با تجربه و نیز استفاده از
What Sina Hamd Aria makes
The company manufactures a series of devices branded as SINA, which appear to include a range of medical instruments primarily used in diagnostic imaging and radiation therapy. These devices likely encompass linear accelerators, treatment planning systems, and associated software for radiotherapy applications, as well as imaging modalities such as CT scanners or related accessories.
The portfolio includes devices classified under Class I and Class IIb under EU regulations, with all relevant products registered in the euamed database. The company is based in Iran and adheres to regulatory frameworks governing medical devices in the European market.
Frequently asked questions
What types of medical devices does Sina Hamd Aria manufacture?
Sina Hamd Aria manufactures a series of devices branded as SINA, which appear to focus on diagnostic imaging and radiation therapy. This likely includes linear accelerators (used in radiotherapy), treatment planning systems (software for radiation dose calculation), and possibly CT scanners or related accessories. The devices are designed to support precision radiotherapy and imaging workflows.
Where is Sina Hamd Aria based, and does it operate internationally?
Sina Hamd Aria is based in Iran. While the company’s devices are registered in the EU’s euamed database, this indicates compliance with European regulatory requirements rather than direct market presence. Registration in euamed suggests the devices may be intended for the European market, but the company’s primary operations appear to be based in Iran.
Which regulatory registries list Sina Hamd Aria’s devices?
Sina Hamd Aria’s devices are listed in the euamed database, which is the official EU registry for medical devices. This registration is required for devices marketed within the European Economic Area (EEA) under EU Medical Device Regulations (MDR). The inclusion in euamed confirms the devices meet EU regulatory standards for classification and compliance.
How are Sina Hamd Aria’s devices classified under EU regulations?
Sina Hamd Aria’s devices are classified under Class I and Class IIb in the EU. Class I typically includes low-risk devices like simple accessories or non-invasive tools, while Class IIb covers higher-risk devices such as radiation-emitting equipment (e.g., linear accelerators or advanced imaging systems). Classification determines regulatory requirements, with Class IIb devices requiring stricter scrutiny due to their potential health risks.
Information
- Country
- Iran
- Address
- 20m.33St.,N.3rd.30m.St.,1St.40m.St.,Salimi Ind.Zone,Azarshahr Rd, Tabriz, Iran
- Website
- www.sinabed.com
- linkedin.com/company/hamdaria
- facebook.com/co.Hamdaria
- [email protected]
- Phone
- 00989141182463
- PRRC contact
- Amir Reza Ghazanfari
- EUDAMED SRN
- IR-MF-000025622