eudamed_udi
Primary ID: 08049033190960
PAR INFUSION (UDI 08049033190960)
Manufactured by Know Medical Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAR INFUSION - Primary ID 08049033190960
Device Regulatory Overview
The PAR INFUSION (Model/Catalog Number: PB015000-O) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A080102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PB015000-O
- Product Code / EMDN
- A080102
- Device Name
- PAR INFUSION - Sacca parenterale 150ml senza set di riempimento
- Database Sync Date
- 2026-08-09 16:29:09
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 PAR INFUSION?
The registered manufacturer of record for PAR INFUSION is Know Medical Srl.
What is the Primary UDI-DI identifier for PAR INFUSION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08049033190960.
What classification code is assigned to this device?
This device is registered under product classification code A080102.
Similar Classification Devices (A080102)
Other Devices by Know Medical Srl
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