gudid
Primary ID: Ochsner endarterectomy dissector
Ambler Surgical (UDI Ochsner endarterectomy dissector)
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 Ochsner endarterectomy dissector
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Ochsner endarterectomy dissector) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Ochsner endarterectomy dissector
- Product Code / EMDN
- GEG
- Device Name
- Ochsner endarterectomy dissector, 7 1/8'', double-ended, curved, 3.0mm/4.0mm wide blades, square handle
- Database Sync Date
- 2026-08-09 09:01:43
Full Regulatory Attributes
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{
"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 Ochsner endarterectomy dissector.
What classification code is assigned to this device?
This device is registered under product classification code GEG.
Similar Classification Devices (GEG)
Other Devices by AMBLER SURGICAL CORP.
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