gudid
Primary ID: Alm retractor
Ambler Surgical (UDI Alm retractor)
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 Alm retractor
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Alm retractor) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification FFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Alm retractor
- Product Code / EMDN
- FFO
- Device Name
- Alm retractor, 2 3/4'', straight, 4x4 blunt prongs, 2'' wide, thumb-screw tension
- Database Sync Date
- 2026-08-09 09:01:47
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 Alm retractor.
What classification code is assigned to this device?
This device is registered under product classification code FFO.
Similar Classification Devices (FFO)
Other Devices by AMBLER SURGICAL CORP.
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