gudid
Primary ID: 1000 ML
LungProtect (UDI 1000 ML)
Manufactured by CARNAMEDICA SP Z O O
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LungProtect - Primary ID 1000 ML
Device Regulatory Overview
The LungProtect (Model/Catalog Number: 1000 ML) is a medical device manufactured by CARNAMEDICA SP Z O O. This product is indexed under FDA Product Code / Category Classification KDN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1000 ML
- Product Code / EMDN
- KDN
- Device Name
- Container filled with solution for perfusion or preservation of organs intended for transplantation.
- Database Sync Date
- 2026-08-09 09:25:00
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 LungProtect?
The registered manufacturer of record for LungProtect is CARNAMEDICA SP Z O O.
What is the Primary UDI-DI identifier for LungProtect?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1000 ML.
What classification code is assigned to this device?
This device is registered under product classification code KDN.
Similar Classification Devices (KDN)
Other Devices by CARNAMEDICA SP Z O O
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint