gudid
Primary ID: 08002
ShotBlocker (UDI 08002)
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 08002
Device Regulatory Overview
The ShotBlocker (Model/Catalog Number: 08002) 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
- 08002
- Product Code / EMDN
- LYG
- Device Name
- 5 ct ShotBlocker
- 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 08002.
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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