gudid
Primary ID: Killian nasal speculum
Ambler Surgical (UDI Killian nasal 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 Surgical - Primary ID Killian nasal speculum
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Killian nasal 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 nasal speculum
- Product Code / EMDN
- EPY
- Device Name
- Killian nasal speculum, 40.0mm blades, with fiberoptics
- 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 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 Killian nasal 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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