gudid
Primary ID: Schmieden ligature guide
Ambler Surgical (UDI Schmieden ligature guide)
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 Schmieden ligature guide
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Schmieden ligature guide) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification FZX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Schmieden ligature guide
- Product Code / EMDN
- FZX
- Device Name
- Schmieden ligature guide, 7 1/4'', 8.0mm wide tip, square 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
}
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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 Schmieden ligature guide.
What classification code is assigned to this device?
This device is registered under product classification code FZX.
Similar Classification Devices (FZX)
Other Devices by AMBLER SURGICAL CORP.
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