gudid
Primary ID: MMT-7510
Enlite Serter (UDI MMT-7510)
Manufactured by MEDTRONIC MINIMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Enlite Serter - Primary ID MMT-7510
Device Regulatory Overview
The Enlite Serter (Model/Catalog Number: MMT-7510) is a medical device manufactured by MEDTRONIC MINIMED, INC.. This product is indexed under FDA Product Code / Category Classification OZO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MMT-7510
- Product Code / EMDN
- OZO
- Device Name
- LANCET DEVICE MMT-7510 ENLT SNSRTR US
- Database Sync Date
- 2026-08-09 09:50:13
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 Enlite Serter?
The registered manufacturer of record for Enlite Serter is MEDTRONIC MINIMED, INC..
What is the Primary UDI-DI identifier for Enlite Serter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MMT-7510.
What classification code is assigned to this device?
This device is registered under product classification code OZO.
Similar Classification Devices (OZO)
Other Devices by MEDTRONIC MINIMED, INC.
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