gudid
Primary ID: 30900
NA (UDI 30900)
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 30900
Device Regulatory Overview
The NA (Model/Catalog Number: 30900) is a medical device manufactured by PANPAC MEDICAL CORPORATION. This product is indexed under FDA Product Code / Category Classification DZE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30900
- Product Code / EMDN
- DZE
- Device Name
- The Pessary Remover is designed for removal of the pessaries easily. It is best used for the removal of the ring, with or without support, the oval, dish, hodge or marland. When using the remover to remove the pessary, it must be used with lubricant.
- Database Sync Date
- 2026-08-09 09:10:27
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 30900.
What classification code is assigned to this device?
This device is registered under product classification code DZE.
Similar Classification Devices (DZE)
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