R SERIES (UDI 30001003101110362)
Manufactured by Zoll Medical Corporation
Device Regulatory Overview
The R SERIES (Model/Catalog Number: 30001003101110362) is a medical device manufactured by Zoll Medical Corporation. This product is indexed under FDA Product Code / Category Classification DPS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening hear...
Technical Specifications
- Model Number
- 30001003101110362
- Product Code / EMDN
- DPS
- Device Name
- Defibrillator ,MAIN, ALS, 3/5 LD, STD ECG, AC PWR, PACE, SPO2, ETCO2, CF/USB, JAPAN
- Database Sync Date
- 2026-08-09 09:15:39
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 R SERIES?
The registered manufacturer of record for R SERIES is Zoll Medical Corporation.
What is the Primary UDI-DI identifier for R SERIES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30001003101110362.
What classification code is assigned to this device?
This device is registered under product classification code DPS.
Similar Classification Devices (DPS)
Other Devices by Zoll Medical Corporation
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