gudid
Primary ID: 706596
Jaeger (UDI 706596)
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 706596
Device Regulatory Overview
The Jaeger (Model/Catalog Number: 706596) 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
- 706596
- Product Code / EMDN
- BXW
- Device Name
- Calibration Syringe 3 Liter
- Database Sync Date
- 2026-08-09 09:17:41
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 706596.
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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