eudamed_udi
Primary ID: 00724995090913
HINGE-FREE (UDI 00724995090913)
Manufactured by STERIS Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HINGE-FREE - Primary ID 00724995090913
Device Regulatory Overview
The HINGE-FREE (Model/Catalog Number: 1031T4PE) is a medical device manufactured by STERIS Corporation. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1031T4PE
- Product Code / EMDN
- D99
- Device Name
- Hinge-Free Instrument Lubricant
- Database Sync Date
- 2026-08-09 16:28:58
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 HINGE-FREE?
The registered manufacturer of record for HINGE-FREE is STERIS Corporation.
What is the Primary UDI-DI identifier for HINGE-FREE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00724995090913.
What classification code is assigned to this device?
This device is registered under product classification code D99.
Similar Classification Devices (D99)
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