gudid
Primary ID: Verbrugge bone holding forceps
Ambler Surgical (UDI Verbrugge bone holding forceps)
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 Verbrugge bone holding forceps
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Verbrugge bone holding forceps) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GEN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Verbrugge bone holding forceps
- Product Code / EMDN
- GEN
- Device Name
- Verbrugge bone holding forceps, 10 1/2'', angled, 11.0mm wide jaws, ring handle with long ratchet
- 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
}
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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 Verbrugge bone holding forceps.
What classification code is assigned to this device?
This device is registered under product classification code GEN.
Similar Classification Devices (GEN)
Other Devices by AMBLER SURGICAL CORP.
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