UDI device identifier
AutoPulse NXT Resuscitation System Model 200
UDI device identifier 00849111003384 · Zoll Circulation, Inc.
Key facts
| Primary DI | 00849111003384 |
|---|---|
| Brand name | AutoPulse NXT Resuscitation System |
| Version or model | Model 200 |
| Catalog number | 8700-001070 |
| Company | Zoll Circulation, Inc. |
| DUNS number | 799455241 |
| Product code | DRM |
| GMDN term | Cardiac resuscitator, line-powered |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 13, 2023 |
| Version date | Oct 23, 2023 |
| Description | The AutoPulse NXT System consists of 4 primary components, a reusable Platform, a single use chest compression assembly (LifeBand), a rechargeable battery, and a battery charger. |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: