eudamed_udi
Primary ID: 07045430076976
Laerdal Silicone Resuscitator (UDI 07045430076976)
Manufactured by Laerdal Medical AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Laerdal Silicone Resuscitator - Primary ID 07045430076976
Device Regulatory Overview
The Laerdal Silicone Resuscitator (Model/Catalog Number: 870702) is a medical device manufactured by Laerdal Medical AS. This product is indexed under FDA Product Code / Category Classification R030280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 870702
- Product Code / EMDN
- R030280
- Device Name
- Laerdal Silicone Resuscitator
- Database Sync Date
- 2026-08-09 18:12:01
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 Laerdal Silicone Resuscitator?
The registered manufacturer of record for Laerdal Silicone Resuscitator is Laerdal Medical AS.
What is the Primary UDI-DI identifier for Laerdal Silicone Resuscitator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07045430076976.
What classification code is assigned to this device?
This device is registered under product classification code R030280.
Similar Classification Devices (R030280)
Other Devices by Laerdal Medical AS
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