gudid
Primary ID: Morse sternal retractor
Ambler Surgical (UDI Morse sternal 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 Morse sternal retractor
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Morse sternal 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
- Morse sternal retractor
- Product Code / EMDN
- DWS
- Device Name
- Morse sternal retractor, adult, 203.0mm x 190.0mm x 29.0mm x 22.0mm
- Database Sync Date
- 2026-08-09 09:01:43
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 Morse sternal 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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