eudamed_udi
Primary ID: 08056215745436
CANNULA ASPIRAZIONE FRAZIER mm4 (UDI 08056215745436)
Manufactured by MEDESY srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CANNULA ASPIRAZIONE FRAZIER mm4 - Primary ID 08056215745436
Device Regulatory Overview
The CANNULA ASPIRAZIONE FRAZIER mm4 (Model/Catalog Number: 911/4) is a medical device manufactured by MEDESY srl. This product is indexed under FDA Product Code / Category Classification L030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 911/4
- Product Code / EMDN
- L030199
- Device Name
- STRUMENTI CHIRURGICI RIUTILIZZABILI
- Database Sync Date
- 2026-08-09 16:51:34
Full Regulatory Attributes
๐ 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 CANNULA ASPIRAZIONE FRAZIER mm4?
The registered manufacturer of record for CANNULA ASPIRAZIONE FRAZIER mm4 is MEDESY srl.
What is the Primary UDI-DI identifier for CANNULA ASPIRAZIONE FRAZIER mm4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056215745436.
What classification code is assigned to this device?
This device is registered under product classification code L030199.
Similar Classification Devices (L030199)
Other Devices by MEDESY srl
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