gudid
Primary ID: 80-6000-50
Bio30+ System Physio Accel (UDI 80-6000-50)
Manufactured by BIOCHROM LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bio30+ System Physio Accel - Primary ID 80-6000-50
Device Regulatory Overview
The Bio30+ System Physio Accel (Model/Catalog Number: 80-6000-50) is a medical device manufactured by BIOCHROM LIMITED. This product is indexed under FDA Product Code / Category Classification JJE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80-6000-50
- Product Code / EMDN
- JJE
- Device Name
- Ion exchange chromatography analyzer with lithium accelerated column, LED monitor, computer, autosampler and Openlab software
- Database Sync Date
- 2026-08-09 09:08:10
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 Bio30+ System Physio Accel?
The registered manufacturer of record for Bio30+ System Physio Accel is BIOCHROM LIMITED.
What is the Primary UDI-DI identifier for Bio30+ System Physio Accel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80-6000-50.
What classification code is assigned to this device?
This device is registered under product classification code JJE.
Similar Classification Devices (JJE)
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