gudid
Primary ID: Ulrich self-retaining bone forceps
Ambler Surgical (UDI Ulrich self-retaining bone 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 Ulrich self-retaining bone forceps
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Ulrich self-retaining bone 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
- Ulrich self-retaining bone forceps
- Product Code / EMDN
- GEN
- Device Name
- Ulrich self-retaining bone forceps, 10'', straight, serrated, 9.0mm wide jaws, speed lock
- 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 Ulrich self-retaining bone 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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