eudamed_udi
Primary ID: 04712568360927
EosStethoscope (UDI 04712568360927)
Manufactured by NORTH EOS INDUSTRIES,INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EosStethoscope - Primary ID 04712568360927
Device Regulatory Overview
The EosStethoscope (Model/Catalog Number: EosStethoscope) is a medical device manufactured by NORTH EOS INDUSTRIES,INC.. This product is indexed under FDA Product Code / Category Classification Z120899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EosStethoscope
- Product Code / EMDN
- Z120899
- Device Name
- EosSpec I
- Database Sync Date
- 2026-08-09 18:39:30
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 EosStethoscope?
The registered manufacturer of record for EosStethoscope is NORTH EOS INDUSTRIES,INC..
What is the Primary UDI-DI identifier for EosStethoscope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712568360927.
What classification code is assigned to this device?
This device is registered under product classification code Z120899.
Similar Classification Devices (Z120899)
Other Devices by NORTH EOS INDUSTRIES,INC.
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