gudid
Primary ID: 2000 Primus HIT Unit
Primus By Auditdata (UDI 2000 Primus HIT Unit)
Manufactured by Auditdata A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Primus By Auditdata - Primary ID 2000 Primus HIT Unit
Device Regulatory Overview
The Primus By Auditdata (Model/Catalog Number: 2000 Primus HIT Unit) is a medical device manufactured by Auditdata A/S. This product is indexed under FDA Product Code / Category Classification ETW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2000 Primus HIT Unit
- Product Code / EMDN
- ETW
- Device Name
- Database Sync Date
- 2026-08-09 09:12:44
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 Primus By Auditdata?
The registered manufacturer of record for Primus By Auditdata is Auditdata A/S.
What is the Primary UDI-DI identifier for Primus By Auditdata?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2000 Primus HIT Unit.
What classification code is assigned to this device?
This device is registered under product classification code ETW.
Similar Classification Devices (ETW)
Other Devices by Auditdata A/S
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