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CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ

Türkiye·TR-MF-000022140

Last updated September 17, 2026

About

Our experienced staff to deliver the products we produce and distribute in a four side of Turkey with continuous and full time, with more than 20 dealers, our business partners and representatives of our international companies, we continue our work without compromising the international quality standards.

Translated from the manufacturer's own website. Source

What CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ makes

The company manufactures single-use manual pulmonary resuscitators and pneumatic general-purpose suction systems, designed for emergency medical and clinical use.

These devices are classified as Class I and Class IIa under EU regulations and are listed in the EUDAQD database (eudamed). The company is based in Turkey.

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 CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ manufacture?

CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ produces two primary types of medical devices: single-use manual pulmonary resuscitators and pneumatic general-purpose suction systems. These devices are designed for emergency medical and clinical use, such as resuscitation and airway management or fluid removal in patient care.

Where is CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ based?

The company is based in Turkey, as indicated by its country designation. This location reflects its operational headquarters and likely regulatory compliance scope.

Which regulatory registries list the devices manufactured by CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ?

The devices produced by the company are listed in the EUDAQD database (eudamed), which is the official European Union registry for medical devices. This listing ensures transparency and traceability of devices under EU regulatory oversight.

How are the devices manufactured by CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ classified under EU regulations?

The devices fall into two classification categories under EU medical device regulations: Class I and Class IIa. Classification depends on factors like risk level, intended use, and patient contact duration—Class IIa indicates a moderate risk requiring additional scrutiny, while Class I typically involves lower-risk devices with basic safety measures.

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

Information

Country
Türkiye
Address
143, 143. Sk., İSTANBUL, Türkiye
LinkedIn
—
Phone
+902124944575
PRRC Contact
Ramazan Haslet DİLLİ
EUDAMED SRN
TR-MF-000022140
FDA FEI Number
—
DUNS Number
—

Catalogue (12)

DeviceModel / ReferenceRegistriesClassStatus
Ccmed 2030-2061
EUDAMED
Class IActive
Exxe 2030-2060
EUDAMED
Class IActive
Ccmed 2030-2060
EUDAMED
Class IActive
Exxe 2030 2061
EUDAMED
Class IActive
Ceren 2030-2061
EUDAMED
Class IActive
Ceren NS 2060 112
EUDAMED
Class IActive
cerenüretim 2024 010
EUDAMED
Class IActive
Ccmed 2030-2062
EUDAMED
Class IActive
Ceren 2030-2060
EUDAMED
Class IActive
Exxe 2030-2062
EUDAMED
Class IActive
Ceren AM 2030 2071
EUDAMED
Class IIaActive
Ceren AS 2030 2072
EUDAMED
Class IIaActive

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