gudid
Primary ID: 20-09490
LFS 1pkg (10pcs) for UDI for Foil Pack 6422 (UDI 20-09490)
Manufactured by Laerdal Medical AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LFS 1pkg (10pcs) for UDI for Foil Pack 6422 - Primary ID 20-09490
Device Regulatory Overview
The LFS 1pkg (10pcs) for UDI for Foil Pack 6422 (Model/Catalog Number: 20-09490) is a medical device manufactured by Laerdal Medical AS. This product is indexed under FDA Product Code / Category Classification BTM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20-09490
- Product Code / EMDN
- BTM
- Device Name
- Laerdal Face Shield (LFS) is a single use medical device intended as a CPR barrier between a rescuer and a patient and to aid rescuers trained in resuscitation, in mouth-to-mouth resuscitation of non-breathing patients.
- Database Sync Date
- 2026-08-09 09:18:19
Full Regulatory Attributes
🔒 Token Gated
{
"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 LFS 1pkg (10pcs) for UDI for Foil Pack 6422?
The registered manufacturer of record for LFS 1pkg (10pcs) for UDI for Foil Pack 6422 is Laerdal Medical AS.
What is the Primary UDI-DI identifier for LFS 1pkg (10pcs) for UDI for Foil Pack 6422?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20-09490.
What classification code is assigned to this device?
This device is registered under product classification code BTM.
Similar Classification Devices (BTM)
Other Devices by Laerdal Medical AS
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