eudamed_udi
Primary ID: 04056839061978
HA PURE 7PX GB (UDI 04056839061978)
Manufactured by Signia GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HA PURE 7PX GB - Primary ID 04056839061978
Device Regulatory Overview
The HA PURE 7PX GB (Model/Catalog Number: 10933857) is a medical device manufactured by Signia GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10933857
- Product Code / EMDN
- Y2145060102
- Device Name
- RIC
- Database Sync Date
- 2026-08-09 16:47:27
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 HA PURE 7PX GB?
The registered manufacturer of record for HA PURE 7PX GB is Signia GmbH.
What is the Primary UDI-DI identifier for HA PURE 7PX GB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056839061978.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060102.
Similar Classification Devices (Y2145060102)
Other Devices by Signia GmbH
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