gudid
Primary ID: 22200
Lighted Ear Curette Demo Pack (UDI 22200)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lighted Ear Curette Demo Pack - Primary ID 22200
Device Regulatory Overview
The Lighted Ear Curette Demo Pack (Model/Catalog Number: 22200) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22200
- Product Code / EMDN
- JYG
- Device Name
- Lighted Ear Curette Demo Pack
- Database Sync Date
- 2026-08-09 09:04:11
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 Lighted Ear Curette Demo Pack?
The registered manufacturer of record for Lighted Ear Curette Demo Pack is Bionix, LLC.
What is the Primary UDI-DI identifier for Lighted Ear Curette Demo Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22200.
What classification code is assigned to this device?
This device is registered under product classification code JYG.
Similar Classification Devices (JYG)
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