gudid
Primary ID: LS-208B
LifeSync (UDI LS-208B)
Manufactured by LifeSync Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LifeSync - Primary ID LS-208B
Device Regulatory Overview
The LifeSync (Model/Catalog Number: LS-208B) is a medical device manufactured by LifeSync Corporation. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LS-208B
- Product Code / EMDN
- DRG
- Device Name
- 12 Lead, LeadWear, size 7L
- Database Sync Date
- 2026-08-09 09:35:45
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 LifeSync?
The registered manufacturer of record for LifeSync is LifeSync Corporation.
What is the Primary UDI-DI identifier for LifeSync?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LS-208B.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
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