gudid
Primary ID: 31-350
Ambler Surgical (UDI 31-350)
Manufactured by AMBLER SURGICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ambler Surgical - Primary ID 31-350
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: 31-350) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification DXC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31-350
- Product Code / EMDN
- DXC
- Device Name
- Johns Hopkins bulldog clamp applying forceps, 9", angled jaws, ring handle
- Database Sync Date
- 2026-08-09 09:01:49
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 Ambler Surgical?
The registered manufacturer of record for Ambler Surgical is AMBLER SURGICAL CORP..
What is the Primary UDI-DI identifier for Ambler Surgical?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31-350.
What classification code is assigned to this device?
This device is registered under product classification code DXC.
Similar Classification Devices (DXC)
Other Devices by AMBLER SURGICAL CORP.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint