gudid
Primary ID: Killian septum speculum
Ambler Value Line (UDI Killian septum speculum)
Manufactured by AMBLER SURGICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ambler Value Line - Primary ID Killian septum speculum
Device Regulatory Overview
The Ambler Value Line (Model/Catalog Number: Killian septum speculum) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification EPY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Killian septum speculum
- Product Code / EMDN
- EPY
- Device Name
- Killian septum speculum, 5 1/2'', size #1, small, 51.0mm blades, with set screw
- Database Sync Date
- 2026-08-09 09:01:43
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 Value Line?
The registered manufacturer of record for Ambler Value Line is AMBLER SURGICAL CORP..
What is the Primary UDI-DI identifier for Ambler Value Line?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Killian septum speculum.
What classification code is assigned to this device?
This device is registered under product classification code EPY.
Similar Classification Devices (EPY)
Other Devices by AMBLER SURGICAL CORP.
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