gudid
Primary ID: XD 2037
N/A (UDI XD 2037)
Manufactured by Ulrich GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID XD 2037
Device Regulatory Overview
The N/A (Model/Catalog Number: XD 2037) is a medical device manufactured by Ulrich GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification IZQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XD 2037
- Product Code / EMDN
- IZQ
- Device Name
- Patient tubing 150 cm for Pump tubing - flex
- Database Sync Date
- 2026-08-09 09:26:12
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 N/A?
The registered manufacturer of record for N/A is Ulrich GmbH & Co. KG.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XD 2037.
What classification code is assigned to this device?
This device is registered under product classification code IZQ.
Similar Classification Devices (IZQ)
Other Devices by Ulrich GmbH & Co. KG
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