gudid
Primary ID: ABI-Q
simpleABI (UDI ABI-Q)
Manufactured by NEWMAN MEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for simpleABI - Primary ID ABI-Q
Device Regulatory Overview
The simpleABI (Model/Catalog Number: ABI-Q) is a medical device manufactured by NEWMAN MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ABI-Q
- Product Code / EMDN
- JAF
- Device Name
- ABI-Q Software, PVR, 2x10cm cuffs, inflation bulb, carry bag, user manual, quick reference guides.
- Database Sync Date
- 2026-08-09 09:49:32
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 simpleABI?
The registered manufacturer of record for simpleABI is NEWMAN MEDICAL LLC.
What is the Primary UDI-DI identifier for simpleABI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ABI-Q.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
Other Devices by NEWMAN MEDICAL LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint