gudid
Primary ID: L250AB
Summit Doppler (UDI L250AB)
Manufactured by Coopersurgical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Summit Doppler - Primary ID L250AB
Device Regulatory Overview
The Summit Doppler (Model/Catalog Number: L250AB) is a medical device manufactured by Coopersurgical, Inc.. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L250AB
- Product Code / EMDN
- JAF
- Device Name
- LifeDop 250 ABI System with 2 Cuffs, Aneroid and Printer
- Database Sync Date
- 2026-08-09 09:19:29
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 Summit Doppler?
The registered manufacturer of record for Summit Doppler is Coopersurgical, Inc..
What is the Primary UDI-DI identifier for Summit Doppler?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L250AB.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
Other Devices by Coopersurgical, Inc.
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