GUDIDData
eudamed_udi Primary ID: 05019829239961

NUBERT New Bag for Endoscopic Retrieval of Tissue (UDI 05019829239961)

Manufactured by Vernacare

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NUBERT New Bag for Endoscopic Retrieval of Tissue - Primary ID 05019829239961

Device Regulatory Overview

The NUBERT New Bag for Endoscopic Retrieval of Tissue (Model/Catalog Number: 24003) is a medical device manufactured by Vernacare. This product is indexed under FDA Product Code / Category Classification A090101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
24003
Product Code / EMDN
A090101
Device Name
Bags for Endoscopic Retrieval of Tissue
Database Sync Date
2026-08-09 18:07:22

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of NUBERT New Bag for Endoscopic Retrieval of Tissue?

The registered manufacturer of record for NUBERT New Bag for Endoscopic Retrieval of Tissue is Vernacare.

What is the Primary UDI-DI identifier for NUBERT New Bag for Endoscopic Retrieval of Tissue?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05019829239961.

What classification code is assigned to this device?

This device is registered under product classification code A090101.

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