gudid
Primary ID: H-410
HolstOR (UDI H-410)
Manufactured by THE O R COMPANY PTY LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HolstOR - Primary ID H-410
Device Regulatory Overview
The HolstOR (Model/Catalog Number: H-410) is a medical device manufactured by THE O R COMPANY PTY LTD. This product is indexed under FDA Product Code / Category Classification MDM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H-410
- Product Code / EMDN
- MDM
- Device Name
- Database Sync Date
- 2026-08-09 09:38:27
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 HolstOR?
The registered manufacturer of record for HolstOR is THE O R COMPANY PTY LTD.
What is the Primary UDI-DI identifier for HolstOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is H-410.
What classification code is assigned to this device?
This device is registered under product classification code MDM.
Similar Classification Devices (MDM)
Other Devices by THE O R COMPANY PTY LTD
Programmatic Export
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