eudamed_udi
Primary ID: 04260237372325
STERIPro Quick NEU (UDI 04260237372325)
Manufactured by Heck Hygiene GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERIPro Quick NEU - Primary ID 04260237372325
Device Regulatory Overview
The STERIPro Quick NEU (Model/Catalog Number: DD323-050) is a medical device manufactured by Heck Hygiene GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DD323-050
- Product Code / EMDN
- D0701
- Device Name
- N.A.
- Database Sync Date
- 2026-08-09 16:49:07
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 STERIPro Quick NEU?
The registered manufacturer of record for STERIPro Quick NEU is Heck Hygiene GmbH.
What is the Primary UDI-DI identifier for STERIPro Quick NEU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260237372325.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
Other Devices by Heck Hygiene GmbH
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