gudid
Primary ID: Unity 3 HIT UNIT US package
Unity 3 (UDI Unity 3 HIT UNIT US package)
Manufactured by Auditdata A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unity 3 - Primary ID Unity 3 HIT UNIT US package
Device Regulatory Overview
The Unity 3 (Model/Catalog Number: Unity 3 HIT UNIT US package) 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
- Unity 3 HIT UNIT US package
- Product Code / EMDN
- ETW
- Device Name
- U3HIT Package AD-version US
- 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 Unity 3?
The registered manufacturer of record for Unity 3 is Auditdata A/S.
What is the Primary UDI-DI identifier for Unity 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Unity 3 HIT UNIT US package.
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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