gudid
Primary ID: 205
SafeStraw 2 Pack (UDI 205)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SafeStraw 2 Pack - Primary ID 205
Device Regulatory Overview
The SafeStraw 2 Pack (Model/Catalog Number: 205) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification ILC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 205
- Product Code / EMDN
- ILC
- Device Name
- SafeStraw 2 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 SafeStraw 2 Pack?
The registered manufacturer of record for SafeStraw 2 Pack is Bionix, LLC.
What is the Primary UDI-DI identifier for SafeStraw 2 Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 205.
What classification code is assigned to this device?
This device is registered under product classification code ILC.
Similar Classification Devices (ILC)
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