gudid
Primary ID: F9053/10
NA (UDI F9053/10)
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 F9053/10
Technical Specifications
- Model Number
- F9053/10
- 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). F9053/10 model are round-shaped electrodes, 32mm, equipped with 10 cm 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.
- Database Sync Date
- 2026-08-09 09:04:39
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 F9053/10.
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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