gudid
Primary ID: UIC5FA
NA (UDI UIC5FA)
Manufactured by PANPAC MEDICAL CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID UIC5FA
Device Regulatory Overview
The NA (Model/Catalog Number: UIC5FA) is a medical device manufactured by PANPAC MEDICAL CORPORATION. This product is indexed under FDA Product Code / Category Classification LKF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UIC5FA
- Product Code / EMDN
- LKF
- Device Name
- The catheter is to be used for sonohysterography procedure that aid in the analysis of uterine pathology. A placement sheath eliminates the need for a tenaculum. This catheter is designed for single patient use.
- Database Sync Date
- 2026-08-09 09:15:29
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 NA?
The registered manufacturer of record for NA is PANPAC MEDICAL CORPORATION.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UIC5FA.
What classification code is assigned to this device?
This device is registered under product classification code LKF.
Similar Classification Devices (LKF)
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