FDA UDI In Commercial Distribution 🇺🇸 United States

Lifecard

DI: 10841522127137 · Model: Lifecard · SPACELABS HEALTHCARE (WASHINGTON), INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lifecard
Primary DI
10841522127137
Version / Model
Lifecard
Catalog Number
LCF4L
Company Name
SPACELABS HEALTHCARE (WASHINGTON), INC
Labeler DUNS
145581588
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-08
Public Version
7
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
47fd0ef6-041b-4680-b7fa-4ce16cb8e921

Device Description

LIFECARD CF, 4 LEAD, HOLTER RECORDER

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWJ Electrocardiograph, ambulatory (without analysis)

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary 10841522127137

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 65 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity