gudid
Primary ID: S4B
CueSee CO-OX (UDI S4B)
Manufactured by Eurotrol B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CueSee CO-OX - Primary ID S4B
Device Regulatory Overview
The CueSee CO-OX (Model/Catalog Number: S4B) is a medical device manufactured by Eurotrol B.V.. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S4B
- Product Code / EMDN
- GGM
- Device Name
- CueSee CO-OX S4B is an unassayed material for professional use containing total hemoglobin (tHb) with fractions of oxygenated hemoglobin (FO2Hb), fractions of carboxyhemoglobin (FCOHb) and fractions of methemoglobin (FMetHb).CueSee CO-OX is intended for professional users (medical and laboratory personnel) in clinical settings (e.g. hospital or laboratory).
- Database Sync Date
- 2026-08-09 09:26:45
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 CueSee CO-OX?
The registered manufacturer of record for CueSee CO-OX is Eurotrol B.V..
What is the Primary UDI-DI identifier for CueSee CO-OX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S4B.
What classification code is assigned to this device?
This device is registered under product classification code GGM.
Similar Classification Devices (GGM)
Other Devices by Eurotrol B.V.
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