eudamed_udi
Primary ID: 05060614530008
Alerta Bubble 2 (UDI 05060614530008)
Manufactured by Alerta Medical Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alerta Bubble 2 - Primary ID 05060614530008
Device Regulatory Overview
The Alerta Bubble 2 (Model/Catalog Number: ALT-9001) is a medical device manufactured by Alerta Medical Ltd. This product is indexed under FDA Product Code / Category Classification V08068099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALT-9001
- Product Code / EMDN
- V08068099
- Device Name
- Alerta Partner Cushion System
- Database Sync Date
- 2026-08-09 16:46:52
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 Alerta Bubble 2?
The registered manufacturer of record for Alerta Bubble 2 is Alerta Medical Ltd.
What is the Primary UDI-DI identifier for Alerta Bubble 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060614530008.
What classification code is assigned to this device?
This device is registered under product classification code V08068099.
Similar Classification Devices (V08068099)
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