gudid
Primary ID: 27220
OtoClear Ear Irrigation System Wands (UDI 27220)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OtoClear Ear Irrigation System Wands - Primary ID 27220
Device Regulatory Overview
The OtoClear Ear Irrigation System Wands (Model/Catalog Number: 27220) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification LRD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 27220
- Product Code / EMDN
- LRD
- Device Name
- Ear Irrigation System Adapter Wands, 3 ct
- Database Sync Date
- 2026-08-09 09:04:11
Full Regulatory Attributes
🔒 Token Gated
{
"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 OtoClear Ear Irrigation System Wands?
The registered manufacturer of record for OtoClear Ear Irrigation System Wands is Bionix, LLC.
What is the Primary UDI-DI identifier for OtoClear Ear Irrigation System Wands?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 27220.
What classification code is assigned to this device?
This device is registered under product classification code LRD.
Similar Classification Devices (LRD)
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