FDA UDI Not in Commercial Distribution 🇺🇸 United States

SENTINEL

DI: 10841522103124 · Model: 98200 · SPACELABS HEALTHCARE (WASHINGTON), INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SENTINEL
Primary DI
10841522103124
Version / Model
98200
Catalog Number
040-1712-00
Company Name
SPACELABS HEALTHCARE (WASHINGTON), INC
Labeler DUNS
145581588
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-13
Public Version
3
Public Version Date
2018-05-15
Public Version Status
Update
Public Device Record Key
5f98b3eb-b113-4dca-9c79-a9d2a87cf678
Distribution End Date
2018-05-15

Device Description

SENTINEL 10 WORKSTATION (X10) + ABP LICENSE

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DQK COMPUTER, DIAGNOSTIC, PROGRAMMABLE

GMDN Terms

Code Name
44098 Cardiology information system application software

Identifiers

Type ID
Primary 10841522103124

Storage Conditions

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