gudid
Primary ID: 227688
Ponto (UDI 227688)
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 227688
Device Regulatory Overview
The Ponto (Model/Catalog Number: 227688) 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
- 227688
- Product Code / EMDN
- LXB
- Device Name
- Softband 5, Unilateral M/L Light Brown
- Database Sync Date
- 2026-08-09 09:12:43
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 227688.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint