eudamed_udi
Primary ID: 08049033199857
BURETTE (UDI 08049033199857)
Manufactured by Know Medical Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BURETTE - Primary ID 08049033199857
Device Regulatory Overview
The BURETTE (Model/Catalog Number: BG150250-O) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A03040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BG150250-O
- Product Code / EMDN
- A03040199
- Device Name
- BLOOD BURETTE - Buretta 150 ml per trasfusione
- Database Sync Date
- 2026-08-09 16:44:57
Full Regulatory Attributes
π 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 BURETTE?
The registered manufacturer of record for BURETTE is Know Medical Srl.
What is the Primary UDI-DI identifier for BURETTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08049033199857.
What classification code is assigned to this device?
This device is registered under product classification code A03040199.
Similar Classification Devices (A03040199)
Other Devices by Know Medical Srl
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