eudamed_udi
Primary ID: 08719327695685
Aerolet (UDI 08719327695685)
Manufactured by Aerolet - Economic Holland B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aerolet - Primary ID 08719327695685
Device Regulatory Overview
The Aerolet (Model/Catalog Number: MO) is a medical device manufactured by Aerolet - Economic Holland B.V.. This product is indexed under FDA Product Code / Category Classification Y183099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MO
- Product Code / EMDN
- Y183099
- Device Name
- Aerolet
- Database Sync Date
- 2026-08-09 18:11:17
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Aerolet?
The registered manufacturer of record for Aerolet is Aerolet - Economic Holland B.V..
What is the Primary UDI-DI identifier for Aerolet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08719327695685.
What classification code is assigned to this device?
This device is registered under product classification code Y183099.
Similar Classification Devices (Y183099)
Other Devices by Aerolet - Economic Holland B.V.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint