MLCL Upgrade (UDI BT21)
Manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
Device Regulatory Overview
The MLCL Upgrade (Model/Catalog Number: BT21) is a medical device manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BT21
- Product Code / EMDN
- DQK
- Device Name
- Upgrade Kit MLCL V7.1
- Database Sync Date
- 2026-08-09 09:35:15
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 MLCL Upgrade?
The registered manufacturer of record for MLCL Upgrade is GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC..
What is the Primary UDI-DI identifier for MLCL Upgrade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BT21.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
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