eudamed_udi
Primary ID: 04048675548072
Vista 120 Non-Inv Model A (UDI 04048675548072)
Manufactured by Drägerwerk AG & Co. KGaA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vista 120 Non-Inv Model A - Primary ID 04048675548072
Device Regulatory Overview
The Vista 120 Non-Inv Model A (Model/Catalog Number: MS34008) is a medical device manufactured by Drägerwerk AG & Co. KGaA. This product is indexed under FDA Product Code / Category Classification Z1203020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MS34008
- Product Code / EMDN
- Z1203020201
- Device Name
- 548072
- Database Sync Date
- 2026-08-09 16:28:46
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 Vista 120 Non-Inv Model A?
The registered manufacturer of record for Vista 120 Non-Inv Model A is Drägerwerk AG & Co. KGaA.
What is the Primary UDI-DI identifier for Vista 120 Non-Inv Model A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048675548072.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020201.
Similar Classification Devices (Z1203020201)
Other Devices by Drägerwerk AG & Co. KGaA
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