gudid
Primary ID: SB-08004
ShotBlocker (UDI SB-08004)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ShotBlocker - Primary ID SB-08004
Device Regulatory Overview
The ShotBlocker (Model/Catalog Number: SB-08004) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification LYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SB-08004
- Product Code / EMDN
- LYG
- Device Name
- ShotBlocker 1,000 ct
- 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 ShotBlocker?
The registered manufacturer of record for ShotBlocker is Bionix, LLC.
What is the Primary UDI-DI identifier for ShotBlocker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SB-08004.
What classification code is assigned to this device?
This device is registered under product classification code LYG.
Similar Classification Devices (LYG)
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