gudid
Primary ID: 7049-6211
DiaSpect Control HBT1 (UDI 7049-6211)
Manufactured by EKF-diagnostic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DiaSpect Control HBT1 - Primary ID 7049-6211
Device Regulatory Overview
The DiaSpect Control HBT1 (Model/Catalog Number: 7049-6211) is a medical device manufactured by EKF-diagnostic GmbH. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7049-6211
- Product Code / EMDN
- GGM
- Device Name
- For the verification of the precision and accuracy of DiaSpect Tm and DiaSpect Tm Cuvettes
- 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 Control HBT1?
The registered manufacturer of record for DiaSpect Control HBT1 is EKF-diagnostic GmbH.
What is the Primary UDI-DI identifier for DiaSpect Control HBT1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7049-6211.
What classification code is assigned to this device?
This device is registered under product classification code GGM.
Similar Classification Devices (GGM)
Other Devices by EKF-diagnostic GmbH
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