EXXE (UDI 08681227076751)
Manufactured by CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The EXXE (Model/Catalog Number: 2030 2061) is a medical device manufactured by CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2030 2061
- Product Code / EMDN
- R03010302
- Device Name
- STERİL OLMAYAN ATOMİZER CHAMBER (ORTA)
- Database Sync Date
- 2026-08-09 17:14:18
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of EXXE?
The registered manufacturer of record for EXXE is CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for EXXE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681227076751.
What classification code is assigned to this device?
This device is registered under product classification code R03010302.
Similar Classification Devices (R03010302)
Other Devices by CEREN ÜRETİM PLASTİK ÜRÜNLERİ SANAYİ TİCARET ANONİM ŞİRKETİ
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