gudid
Primary ID: 7049-3013-0369
DiaSpect Tm Cuvettes (UDI 7049-3013-0369)
Manufactured by EKF-diagnostic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DiaSpect Tm Cuvettes - Primary ID 7049-3013-0369
Device Regulatory Overview
The DiaSpect Tm Cuvettes (Model/Catalog Number: 7049-3013-0369) is a medical device manufactured by EKF-diagnostic GmbH. This product is indexed under FDA Product Code / Category Classification GKR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7049-3013-0369
- Product Code / EMDN
- GKR
- Device Name
- For the quantitative determination of hemoglobin in whole blood.
- Database Sync Date
- 2026-08-09 09:29:22
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 DiaSpect Tm Cuvettes?
The registered manufacturer of record for DiaSpect Tm Cuvettes is EKF-diagnostic GmbH.
What is the Primary UDI-DI identifier for DiaSpect Tm Cuvettes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7049-3013-0369.
What classification code is assigned to this device?
This device is registered under product classification code GKR.
Similar Classification Devices (GKR)
Other Devices by EKF-diagnostic GmbH
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