gudid
Primary ID: 235649
Ponto (UDI 235649)
Manufactured by Oticon Medical AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ponto - Primary ID 235649
Device Regulatory Overview
The Ponto (Model/Catalog Number: 235649) is a medical device manufactured by Oticon Medical AB. This product is indexed under FDA Product Code / Category Classification LXB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 235649
- Product Code / EMDN
- LXB
- Device Name
- Genie Medical BAHS 2022.1 DVD.ISO file for this software is 5712149026999
- Database Sync Date
- 2026-08-09 09:12:43
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 Ponto?
The registered manufacturer of record for Ponto is Oticon Medical AB.
What is the Primary UDI-DI identifier for Ponto?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 235649.
What classification code is assigned to this device?
This device is registered under product classification code LXB.
Similar Classification Devices (LXB)
Other Devices by Oticon Medical AB
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