gudid
Primary ID: 25-771-D45
Ambler Surgical (UDI 25-771-D45)
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 25-771-D45
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: 25-771-D45) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 25-771-D45
- Product Code / EMDN
- GEI
- Device Name
- MicroGlide MIS bipolar forceps, 5 1/2", working length 1 1/2", bayonet shafts, curved down 45, 0.7mm wide non-stick tips, with guide stop, insulated, flat handle
- Database Sync Date
- 2026-08-09 09:01:44
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 25-771-D45.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by AMBLER SURGICAL CORP.
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