FDA UDI In Commercial Distribution 🇺🇸 United States

CardioPulse Go

DI: 07613365003789 · Model: 3.900871 · Schiller AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CardioPulse Go
Primary DI
07613365003789
Version / Model
3.900871
Catalog Number
98320
Company Name
Schiller AG
Labeler DUNS
480868538
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-05
Public Version
1
Public Version Date
2021-11-15
Public Version Status
New
Public Device Record Key
0e152e15-dd54-45d6-99ea-62c228ddcf70

Device Description

The CardioPulse Go is a 12-lead ECG device used for the recording, analysis and evaluation of ECG recordings.

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
MR Unsafe
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
DPS Electrocardiograph

GMDN Terms

Code Name
16231 Electrocardiograph, professional, multichannel

Identifiers

Type ID
Primary 07613365003789

Customer Contacts

Phone
+41417664242

Premarket Submissions

Submission Number Supplement Number
K170182 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
5 – 50 Degrees Celsius