eudamed_udi
Primary ID: 04057155000948
ERT PT (UDI 04057155000948)
Manufactured by eResearchTechnology GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERT PT - Primary ID 04057155000948
Device Regulatory Overview
The ERT PT (Model/Catalog Number: 706000) is a medical device manufactured by eResearchTechnology GmbH. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 706000
- Product Code / EMDN
- Z12150101
- Device Name
- SpiroSphere
- Database Sync Date
- 2026-08-09 16:48:25
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 ERT PT?
The registered manufacturer of record for ERT PT is eResearchTechnology GmbH.
What is the Primary UDI-DI identifier for ERT PT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04057155000948.
What classification code is assigned to this device?
This device is registered under product classification code Z12150101.
Similar Classification Devices (Z12150101)
Other Devices by eResearchTechnology GmbH
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