gudid
Primary ID: 2651
Microsuction Replacement Pack (UDI 2651)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Microsuction Replacement Pack - Primary ID 2651
Device Regulatory Overview
The Microsuction Replacement Pack (Model/Catalog Number: 2651) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2651
- Product Code / EMDN
- JZF
- Device Name
- Microsuction Replacement Pack
- Database Sync Date
- 2026-08-09 09:04:11
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Microsuction Replacement Pack?
The registered manufacturer of record for Microsuction Replacement Pack is Bionix, LLC.
What is the Primary UDI-DI identifier for Microsuction Replacement Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2651.
What classification code is assigned to this device?
This device is registered under product classification code JZF.
Similar Classification Devices (JZF)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint