Battery module (UDI 6889000)
Manufactured by Maquet Critical Care AB
Device Regulatory Overview
The Battery module (Model/Catalog Number: 6889000) is a medical device manufactured by Maquet Critical Care AB. This product is indexed under FDA Product Code / Category Classification MNT within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 6889000
- Product Code / EMDN
- MNT
- Device Name
- Database Sync Date
- 2026-08-09 09:10:28
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 Battery module?
The registered manufacturer of record for Battery module is Maquet Critical Care AB.
What is the Primary UDI-DI identifier for Battery module?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6889000.
What classification code is assigned to this device?
This device is registered under product classification code MNT.
Similar Classification Devices (MNT)
Other Devices by Maquet Critical Care AB
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