gudid
Primary ID: 3
Exer Scan (UDI 3)
Manufactured by Exer Labs, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Exer Scan - Primary ID 3
Device Regulatory Overview
The Exer Scan (Model/Catalog Number: 3) is a medical device manufactured by Exer Labs, Inc.. This product is indexed under FDA Product Code / Category Classification ISD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3
- Product Code / EMDN
- ISD
- Device Name
- Database Sync Date
- 2026-08-09 09:04:00
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 Exer Scan?
The registered manufacturer of record for Exer Scan is Exer Labs, Inc..
What is the Primary UDI-DI identifier for Exer Scan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3.
What classification code is assigned to this device?
This device is registered under product classification code ISD.
Similar Classification Devices (ISD)
Other Devices by Exer Labs, Inc.
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