gudid
Primary ID: 710602
NA (UDI 710602)
Manufactured by US Endoscopy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 710602
Device Regulatory Overview
The NA (Model/Catalog Number: 710602) is a medical device manufactured by US Endoscopy. This product is indexed under FDA Product Code / Category Classification FCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 710602
- Product Code / EMDN
- FCX
- Device Name
- The Two tank shuttle valve system is for use with an insufflator to attach two medical grade CO2 cylinders simultaneously. This reduces the likelihood of running out of CO2 during a procedure.
- Database Sync Date
- 2026-08-09 09:19:09
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 NA?
The registered manufacturer of record for NA is US Endoscopy.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 710602.
What classification code is assigned to this device?
This device is registered under product classification code FCX.
Similar Classification Devices (FCX)
Other Devices by US Endoscopy
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint