gudid
Primary ID: Moberg retractor
Ambler Surgical (UDI Moberg 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 Moberg retractor
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Moberg retractor) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification DWS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Moberg retractor
- Product Code / EMDN
- DWS
- Device Name
- Moberg retractor, 6 3/4'', angled 90 degrees, 5.0mm x 12.0mm blade, 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 Moberg retractor.
What classification code is assigned to this device?
This device is registered under product classification code DWS.
Similar Classification Devices (DWS)
Other Devices by AMBLER SURGICAL CORP.
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