gudid
Primary ID: 2205-0000
Alaris (UDI 2205-0000)
Manufactured by BD Switzerland Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alaris - Primary ID 2205-0000
Device Regulatory Overview
The Alaris (Model/Catalog Number: 2205-0000) is a medical device manufactured by BD Switzerland Srl. This product is indexed under FDA Product Code / Category Classification LZH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2205-0000
- Product Code / EMDN
- LZH
- Device Name
- Alaris Pump Module Enteral Set
- Database Sync Date
- 2026-08-09 09:16:32
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 Alaris?
The registered manufacturer of record for Alaris is BD Switzerland Srl.
What is the Primary UDI-DI identifier for Alaris?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2205-0000.
What classification code is assigned to this device?
This device is registered under product classification code LZH.
Similar Classification Devices (LZH)
Other Devices by BD Switzerland Srl
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