gudid
Primary ID: Freimuth ear curette
Ambler Surgical (UDI Freimuth ear curette)
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 Freimuth ear curette
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Freimuth ear curette) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Freimuth ear curette
- Product Code / EMDN
- JYG
- Device Name
- Freimuth ear curette, 6 1/4'', 2.3mm x 4.5mm serrated loop
- Database Sync Date
- 2026-08-09 09:01:44
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 Freimuth ear curette.
What classification code is assigned to this device?
This device is registered under product classification code JYG.
Similar Classification Devices (JYG)
Other Devices by AMBLER SURGICAL CORP.
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