Sümer (UDI 08698918582255)
Manufactured by SÜMER ULUSLARARASI SANAYİ VE TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The Sümer (Model/Catalog Number: ---) is a medical device manufactured by SÜMER ULUSLARARASI SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Z12011304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ---
- Product Code / EMDN
- Z12011304
- Device Name
- SM-2 CKK Çift Kayar Kapak Prizmatik Otoklav Sterilizatörü 400 L
- Database Sync Date
- 2026-08-09 16:44:52
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 Sümer?
The registered manufacturer of record for Sümer is SÜMER ULUSLARARASI SANAYİ VE TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Sümer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698918582255.
What classification code is assigned to this device?
This device is registered under product classification code Z12011304.
Similar Classification Devices (Z12011304)
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