GUDIDData
gudid Primary ID: 8810-NK

Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit (UDI 8810-NK)

Manufactured by B.L.S. Systems Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit - Primary ID 8810-NK

Device Regulatory Overview

The Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit (Model/Catalog Number: 8810-NK) is a medical device manufactured by B.L.S. Systems Limited. This product is indexed under FDA Product Code / Category Classification BYE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8810-NK
Product Code / EMDN
BYE
Device Name
Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit
Database Sync Date
2026-08-09 09:16:44

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit?

The registered manufacturer of record for Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit is B.L.S. Systems Limited.

What is the Primary UDI-DI identifier for Rescuer II Compact CPAP System with Small Deluxe CPAP Mask and Nebulizer Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8810-NK.

What classification code is assigned to this device?

This device is registered under product classification code BYE.

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