gudid
Primary ID: 5701322
Henry Schein (UDI 5701322)
Manufactured by HENRY SCHEIN, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Henry Schein - Primary ID 5701322
Device Regulatory Overview
The Henry Schein (Model/Catalog Number: 5701322) is a medical device manufactured by HENRY SCHEIN, INC.. This product is indexed under FDA Product Code / Category Classification GKR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5701322
- Product Code / EMDN
- GKR
- Device Name
- OneStepTM + Pro Hb Optical System Check
- Database Sync Date
- 2026-08-09 09:20:12
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 Henry Schein?
The registered manufacturer of record for Henry Schein is HENRY SCHEIN, INC..
What is the Primary UDI-DI identifier for Henry Schein?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5701322.
What classification code is assigned to this device?
This device is registered under product classification code GKR.
Similar Classification Devices (GKR)
Other Devices by HENRY SCHEIN, INC.
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