ECG 5 lead Grabber, IEC + SpO2, Tele (UDI 00884838119109)
Manufactured by Philips Medizin Systeme Böblingen GmbH
Device Regulatory Overview
The ECG 5 lead Grabber, IEC + SpO2, Tele (Model/Catalog Number: 989803171951) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1203020280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 989803171951
- Product Code / EMDN
- Z1203020280
- Device Name
- Lead sets w/wo SpO2 adapter and Cables
- Database Sync Date
- 2026-08-09 16:47:29
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ECG 5 lead Grabber, IEC + SpO2, Tele?
The registered manufacturer of record for ECG 5 lead Grabber, IEC + SpO2, Tele is Philips Medizin Systeme Böblingen GmbH.
What is the Primary UDI-DI identifier for ECG 5 lead Grabber, IEC + SpO2, Tele?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838119109.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020280.
Similar Classification Devices (Z1203020280)
Other Devices by Philips Medizin Systeme Böblingen GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint