DORO LUCENT iMRI Transfer Collision Indicator (UDI 4003.126)
Manufactured by Black Forest Medical GmbH
Device Regulatory Overview
The DORO LUCENT iMRI Transfer Collision Indicator (Model/Catalog Number: 4003.126) is a medical device manufactured by Black Forest Medical GmbH. This product is indexed under FDA Product Code / Category Classification HBM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4003.126
- Product Code / EMDN
- HBM
- Device Name
- DORO LUCENT iMRI Transfer Collision Indicator 700 MAQUET Otesus+Alphamaquet, US to SIEMENS
- Database Sync Date
- 2026-08-09 09:17:45
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 DORO LUCENT iMRI Transfer Collision Indicator?
The registered manufacturer of record for DORO LUCENT iMRI Transfer Collision Indicator is Black Forest Medical GmbH.
What is the Primary UDI-DI identifier for DORO LUCENT iMRI Transfer Collision Indicator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4003.126.
What classification code is assigned to this device?
This device is registered under product classification code HBM.
Similar Classification Devices (HBM)
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