gudid
Primary ID: Farabeuf periosteal raspatory
Ambler Surgical (UDI Farabeuf periosteal raspatory)
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 Farabeuf periosteal raspatory
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Farabeuf periosteal raspatory) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GAC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Farabeuf periosteal raspatory
- Product Code / EMDN
- GAC
- Device Name
- Farabeuf periosteal raspatory, 6'', curved, 13.0mm wide, sharp blade, flat handle
- Database Sync Date
- 2026-08-09 09:01:47
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 Farabeuf periosteal raspatory.
What classification code is assigned to this device?
This device is registered under product classification code GAC.
Similar Classification Devices (GAC)
Other Devices by AMBLER SURGICAL CORP.
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