gudid
Primary ID: V-720252-13
Jaeger (UDI V-720252-13)
Manufactured by Jaeger Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Jaeger - Primary ID V-720252-13
Device Regulatory Overview
The Jaeger (Model/Catalog Number: V-720252-13) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BXW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V-720252-13
- Product Code / EMDN
- BXW
- Device Name
- Calibration Syringe 1 L
- Database Sync Date
- 2026-08-09 09:59:20
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 Jaeger?
The registered manufacturer of record for Jaeger is Jaeger Medical GmbH.
What is the Primary UDI-DI identifier for Jaeger?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V-720252-13.
What classification code is assigned to this device?
This device is registered under product classification code BXW.
Similar Classification Devices (BXW)
Other Devices by Jaeger Medical GmbH
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