gudid
Primary ID: HD+
HD (UDI HD+)
Manufactured by INTEROJO INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HD - Primary ID HD+
Device Regulatory Overview
The HD (Model/Catalog Number: HD+) is a medical device manufactured by INTEROJO INC.. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HD+
- Product Code / EMDN
- DRG
- Device Name
- Digital portable acquisition device which can acquire the electrocardiographic signal of 12 standard leads. Connected with a receiver via Bluetooth, sends the data to the host.
- Database Sync Date
- 2026-08-09 09:04:28
Full Regulatory Attributes
🔒 Token Gated
{
"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 HD?
The registered manufacturer of record for HD is INTEROJO INC..
What is the Primary UDI-DI identifier for HD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HD+.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by INTEROJO INC.
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