gudid
Primary ID: 8900
Rescuer Nebulizer Kit for CPAP Systems (UDI 8900)
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 Nebulizer Kit for CPAP Systems - Primary ID 8900
Device Regulatory Overview
The Rescuer Nebulizer Kit for CPAP Systems (Model/Catalog Number: 8900) is a medical device manufactured by B.L.S. Systems Limited. This product is indexed under FDA Product Code / Category Classification CCQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8900
- Product Code / EMDN
- CCQ
- Device Name
- Rescuer Nebulizer Kit for 8700 and 8800 series CPAP Systems
- 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 Nebulizer Kit for CPAP Systems?
The registered manufacturer of record for Rescuer Nebulizer Kit for CPAP Systems is B.L.S. Systems Limited.
What is the Primary UDI-DI identifier for Rescuer Nebulizer Kit for CPAP Systems?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8900.
What classification code is assigned to this device?
This device is registered under product classification code CCQ.
Similar Classification Devices (CCQ)
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