FDA UDI In Commercial Distribution 🇺🇸 United States

SENTINEL

DI: 10841522100710 · Model: 98200 · SPACELABS HEALTHCARE (WASHINGTON), INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SENTINEL
Primary DI
10841522100710
Version / Model
98200
Catalog Number
98200 v10.0
Company Name
SPACELABS HEALTHCARE (WASHINGTON), INC
Labeler DUNS
145581588
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-13
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1ae3c071-2b5e-4028-b8e9-58fa2909b6cf

Device Description

SENTINEL

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXH TRANSMITTERS AND RECEIVERS, ELECTROCARDIOGRAPH, TELEPHONE

GMDN Terms

Code Name
44098 Cardiology information system application software

Identifiers

Type ID
Primary 10841522100710

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 0 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 0 Degrees Celsius