gudid
Primary ID: 173100
Jaeger (UDI 173100)
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 173100
Device Regulatory Overview
The Jaeger (Model/Catalog Number: 173100) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 173100
- Product Code / EMDN
- BZC
- Device Name
- MasterScreen CPX
- 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 173100.
What classification code is assigned to this device?
This device is registered under product classification code BZC.
Similar Classification Devices (BZC)
Other Devices by Jaeger Medical GmbH
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