Rescuer Emergency CPAP with Nebulizer Kit (UDI 8700-NK)
Manufactured by B.L.S. Systems Limited
Device Regulatory Overview
The Rescuer Emergency CPAP with Nebulizer Kit (Model/Catalog Number: 8700-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
- 8700-NK
- Product Code / EMDN
- BYE
- Device Name
- Rescuer Emergency CPAP with Large Adult CPAP Mask and enclosed nebulizer kit (8900)
- Database Sync Date
- 2026-08-09 09:16:44
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 Rescuer Emergency CPAP with Nebulizer Kit?
The registered manufacturer of record for Rescuer Emergency CPAP with Nebulizer Kit is B.L.S. Systems Limited.
What is the Primary UDI-DI identifier for Rescuer Emergency CPAP with Nebulizer Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8700-NK.
What classification code is assigned to this device?
This device is registered under product classification code BYE.
Similar Classification Devices (BYE)
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