FDA UDI In Commercial Distribution 🇺🇸 United States

Flexport

DI: 10841522105142 · Model: Flexport · SPACELABS HEALTHCARE (WASHINGTON), INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Flexport
Primary DI
10841522105142
Version / Model
Flexport
Catalog Number
90436A-15
Company Name
SPACELABS HEALTHCARE (WASHINGTON), INC
Labeler DUNS
145581588
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-10
Public Version
8
Public Version Date
2023-10-26
Public Version Status
Update
Public Device Record Key
5300329e-d25c-41a7-bb46-e747abe746a6

Device Description

T/A,FLEXPORT,PB840,VENTILATOR INTERFACE

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
DQA Oximeter

GMDN Terms

Code Name
36862 Patient monitoring system module, interfacing

Identifiers

Type ID
Primary 10841522105142

Premarket Submissions

Submission Number Supplement Number
K903702 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 75 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity