gudid
Primary ID: Kuhn frontal sinus seeker
Ambler Surgical (UDI Kuhn frontal sinus seeker)
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 Kuhn frontal sinus seeker
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Kuhn frontal sinus seeker) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification KAK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Kuhn frontal sinus seeker
- Product Code / EMDN
- KAK
- Device Name
- Kuhn frontal sinus seeker, double-ended, size #2, hexagonal handle
- Database Sync Date
- 2026-08-09 09:01:49
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 Kuhn frontal sinus seeker.
What classification code is assigned to this device?
This device is registered under product classification code KAK.
Similar Classification Devices (KAK)
Other Devices by AMBLER SURGICAL CORP.
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