FDA UDI In Commercial Distribution 🇺🇸 United States

AutoPulse®Resuscitation System

DI: 00849111000970 · Model: 100 · Zoll Circulation, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AutoPulse®Resuscitation System
Primary DI
00849111000970
Version / Model
100
Catalog Number
8700-0730-27-66
Company Name
Zoll Circulation, Inc.
Labeler DUNS
799455241
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
642ee110-f5d2-491e-8592-393b9121bb6d

Device Description

The AutoPulse System consists of 4 primary components, a reusable Platform, a single use chest compression assembly (LifeBand), a rechargeable battery, and a battery charger.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRM Compressor, Cardiac, External

GMDN Terms

Code Name
44780 Cardiac resuscitator, line-powered

Identifiers

Type ID
Primary 00849111000970

Customer Contacts

Phone
4085412140

Premarket Submissions

Submission Number Supplement Number
K112998 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 149 Degrees Fahrenheit