gudid
Primary ID: 7122
N/A (UDI 7122)
Manufactured by PENTAX OF AMERICA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 7122
Device Regulatory Overview
The N/A (Model/Catalog Number: 7122) is a medical device manufactured by PENTAX OF AMERICA, INC.. This product is indexed under FDA Product Code / Category Classification GFF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7122
- Product Code / EMDN
- GFF
- Device Name
- EMG Transducers (two channel)
- Database Sync Date
- 2026-08-09 09:07:42
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 N/A?
The registered manufacturer of record for N/A is PENTAX OF AMERICA, INC..
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7122.
What classification code is assigned to this device?
This device is registered under product classification code GFF.
Similar Classification Devices (GFF)
Other Devices by PENTAX OF AMERICA, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint