gudid
Primary ID: 1301-515
ENDOLARYNGEAL PROBE (UDI 1301-515)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ENDOLARYNGEAL PROBE - Primary ID 1301-515
Device Regulatory Overview
The ENDOLARYNGEAL PROBE (Model/Catalog Number: 1301-515) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification KAK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1301-515
- Product Code / EMDN
- KAK
- Device Name
- ENDOLARYNGEAL PROBE MICROSCOPIC STRAIGHT BUTTON-END
- Database Sync Date
- 2026-08-09 09:07:04
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 ENDOLARYNGEAL PROBE?
The registered manufacturer of record for ENDOLARYNGEAL PROBE is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for ENDOLARYNGEAL PROBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1301-515.
What classification code is assigned to this device?
This device is registered under product classification code KAK.
Similar Classification Devices (KAK)
Other Devices by SONTEC INSTRUMENTS, INC.
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