gudid
Primary ID: 3HD4.40P
BaseVac (UDI 3HD4.40P)
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 3HD4.40P
Device Regulatory Overview
The BaseVac (Model/Catalog Number: 3HD4.40P) 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
- 3HD4.40P
- Product Code / EMDN
- NRD
- Device Name
- 12 User Triple Pump Package | 230V 2Hp (x3) w/ 12 Gal Air Water Separator
- Database Sync Date
- 2026-08-09 09:01:55
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 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 3HD4.40P.
What classification code is assigned to this device?
This device is registered under product classification code NRD.
Similar Classification Devices (NRD)
Other Devices by R. E. Morrison Equipment Inc
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