gudid
Primary ID: 27275
27275 (UDI 27275)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 27275 - Primary ID 27275
Device Regulatory Overview
The 27275 (Model/Catalog Number: 27275) 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
- 27275
- Product Code / EMDN
- LRD
- Device Name
- OtoClear Aquabot Sample
- 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 27275?
The registered manufacturer of record for 27275 is Bionix, LLC.
What is the Primary UDI-DI identifier for 27275?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 27275.
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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