eudamed_udi
Primary ID: 08053847360853
BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL) (UDI 08053847360853)
Manufactured by GINEVRI srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL) - Primary ID 08053847360853
Device Regulatory Overview
The BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL) (Model/Catalog Number: 11659H73) is a medical device manufactured by GINEVRI srl. This product is indexed under FDA Product Code / Category Classification T0207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11659H73
- Product Code / EMDN
- T0207
- Device Name
- BONNET for NIV
- Database Sync Date
- 2026-08-09 16:47:23
Full Regulatory Attributes
🔒 Token Gated
{
"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 BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL)?
The registered manufacturer of record for BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL) is GINEVRI srl.
What is the Primary UDI-DI identifier for BONNET for NIV - LARGE SIZES KIT (2M, 2L, 2XL)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053847360853.
What classification code is assigned to this device?
This device is registered under product classification code T0207.
Similar Classification Devices (T0207)
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