GUDIDData
gudid Primary ID: 2SUR4.16-3

BaseVac (UDI 2SUR4.16-3)

Manufactured by R. E. Morrison Equipment Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BaseVac - Primary ID 2SUR4.16-3

Device Regulatory Overview

The BaseVac (Model/Catalog Number: 2SUR4.16-3) is a medical device manufactured by R. E. Morrison Equipment Inc. This product is indexed under FDA Product Code / Category Classification NRD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2SUR4.16-3
Product Code / EMDN
NRD
Device Name
Dual Surgical Vac Pump Package | NFPA Cat 3 | 3 User 0.94 Hp (x2) w/ 20 Gal Receiver
Database Sync Date
2026-08-09 09:01:55

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 BaseVac?

The registered manufacturer of record for BaseVac is R. E. Morrison Equipment Inc.

What is the Primary UDI-DI identifier for BaseVac?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2SUR4.16-3.

What classification code is assigned to this device?

This device is registered under product classification code NRD.

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