gudid
Primary ID: 033-10-072U
Venticaire Lite (UDI 033-10-072U)
Manufactured by FLEXICARE MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Venticaire Lite - Primary ID 033-10-072U
Device Regulatory Overview
The Venticaire Lite (Model/Catalog Number: 033-10-072U) is a medical device manufactured by FLEXICARE MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification KGB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 033-10-072U
- Product Code / EMDN
- KGB
- Device Name
- Adult Non Rebreathing Mask with Head Strap and 2.1m Oxygen Tubing
- Database Sync Date
- 2026-08-09 09:08:16
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 Venticaire Lite?
The registered manufacturer of record for Venticaire Lite is FLEXICARE MEDICAL LIMITED.
What is the Primary UDI-DI identifier for Venticaire Lite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 033-10-072U.
What classification code is assigned to this device?
This device is registered under product classification code KGB.
Similar Classification Devices (KGB)
Other Devices by FLEXICARE MEDICAL LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint