AVANOS (UDI 98706)
Manufactured by Avanos Medical, Inc.
Device Regulatory Overview
The AVANOS (Model/Catalog Number: 98706) is a medical device manufactured by Avanos Medical, Inc.. This product is indexed under FDA Product Code / Category Classification KGC within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 98706
- Product Code / EMDN
- KGC
- Device Name
- Enteral Access Dilation System
- Database Sync Date
- 2026-08-09 09:20:09
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 AVANOS?
The registered manufacturer of record for AVANOS is Avanos Medical, Inc..
What is the Primary UDI-DI identifier for AVANOS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 98706.
What classification code is assigned to this device?
This device is registered under product classification code KGC.
Similar Classification Devices (KGC)
Other Devices by Avanos Medical, Inc.
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