gudid
Primary ID: 570187-2
Suction bag, single packed, 3000 ml (UDI 570187-2)
Manufactured by Serres Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Suction bag, single packed, 3000 ml - Primary ID 570187-2
Device Regulatory Overview
The Suction bag, single packed, 3000 ml (Model/Catalog Number: 570187-2) is a medical device manufactured by Serres Oy. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 570187-2
- Product Code / EMDN
- KDQ
- Device Name
- Database Sync Date
- 2026-08-09 09:24:56
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 Suction bag, single packed, 3000 ml?
The registered manufacturer of record for Suction bag, single packed, 3000 ml is Serres Oy.
What is the Primary UDI-DI identifier for Suction bag, single packed, 3000 ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 570187-2.
What classification code is assigned to this device?
This device is registered under product classification code KDQ.
Similar Classification Devices (KDQ)
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