gudid
Primary ID: F9053PRRM
NA (UDI F9053PRRM)
Manufactured by FIAB SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID F9053PRRM
Technical Specifications
- Model Number
- F9053PRRM
- Product Code / EMDN
- DRX
- Device Name
- Disposable ECG monitoring electrodes have features that make them absolutely reliable during long monitoring ECG recording (not longer than 72 hours). F9053PRRM model are oval-shaped electrodes, 20x15mm dimensions, equipped with 35cm long wire and 4mm socket, pre-gelled and they can be easily connected to the ECG monitor, avoiding pressure on the skin. The external layer in waterproof medical grade PE foam protects the skin beneath the electrode from air and contaminating fluids.F9053PRRM model is radiotranslucent, therefore it allows the user to perform radiographic procedures without removing the electrode.
- Database Sync Date
- 2026-08-09 09:04:31
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 NA?
The registered manufacturer of record for NA is FIAB SPA.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F9053PRRM.
What classification code is assigned to this device?
This device is registered under product classification code DRX.
Similar Classification Devices (DRX)
Other Devices by FIAB SPA
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