PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE (UDI 63050106 rev. F)
Manufactured by CARDIOLINE SPA
Device Regulatory Overview
The PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE (Model/Catalog Number: 63050106 rev. F) is a medical device manufactured by CARDIOLINE SPA. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 63050106 rev. F
- Product Code / EMDN
- DRG
- Device Name
- Patient cable plug AHA cleared with HD+12 and HD+15
- Database Sync Date
- 2026-08-09 09:04:28
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 PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE?
The registered manufacturer of record for PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE is CARDIOLINE SPA.
What is the Primary UDI-DI identifier for PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 63050106 rev. F.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by CARDIOLINE SPA
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