gudid
Primary ID: Patient
LEVO (UDI Patient)
Manufactured by OTOHARMONICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LEVO - Primary ID Patient
Device Regulatory Overview
The LEVO (Model/Catalog Number: Patient) is a medical device manufactured by OTOHARMONICS CORPORATION. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Patient
- Product Code / EMDN
- KLW
- Device Name
- Database Sync Date
- 2026-08-09 09:04:00
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 LEVO?
The registered manufacturer of record for LEVO is OTOHARMONICS CORPORATION.
What is the Primary UDI-DI identifier for LEVO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Patient.
What classification code is assigned to this device?
This device is registered under product classification code KLW.
Similar Classification Devices (KLW)
Other Devices by OTOHARMONICS CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint