gudid
Primary ID: OB23
Ora-Aid (UDI OB23)
Manufactured by TBM Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ora-Aid - Primary ID OB23
Device Regulatory Overview
The Ora-Aid (Model/Catalog Number: OB23) is a medical device manufactured by TBM Corporation. This product is indexed under FDA Product Code / Category Classification OLR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OB23
- Product Code / EMDN
- OLR
- Device Name
- Database Sync Date
- 2026-08-09 09:28:52
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 Ora-Aid?
The registered manufacturer of record for Ora-Aid is TBM Corporation.
What is the Primary UDI-DI identifier for Ora-Aid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is OB23.
What classification code is assigned to this device?
This device is registered under product classification code OLR.
Similar Classification Devices (OLR)
Other Devices by TBM Corporation
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