gudid
Primary ID: BA051F
NA (UDI BA051F)
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 BA051F
Device Regulatory Overview
The NA (Model/Catalog Number: BA051F) 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
- BA051F
- Product Code / EMDN
- LKF
- Device Name
- HSG catheter sets can be used for sonohysterography and hysterosalpingography procedures that greatly enhance the analysis of uterine pathology. Using HSG balloon catheters, the procedures are simple and non-traumatic for your patients. A placement sheath eliminates the need for a tenaculum. HSG catheters are designed for single patient use only.
- Database Sync Date
- 2026-08-09 09:15:29
Full Regulatory Attributes
🔒 Token Gated
{
"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 BA051F.
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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