FDA UDI In Commercial Distribution 🇺🇸 United States

Xper Flex Cardio Physiomonitoring System

DI: 00884838103245 · Model: Xper Flex Cardio FC2010 REV C Russian · Philips Ds North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Xper Flex Cardio Physiomonitoring System
Primary DI
00884838103245
Version / Model
Xper Flex Cardio FC2010 REV C Russian
Catalog Number
453564675011
Company Name
Philips Ds North America LLC
Labeler DUNS
013649151
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-30
Public Version
6
Public Version Date
2024-02-01
Public Version Status
Update
Public Device Record Key
543ef400-a336-4c23-ac4b-7b7d7519eee5

Device Description

Xper Flex Cardio FC2010 REV C Russian

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWI Monitor, physiological, patient (without arrhythmia detection or alarms)

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 00884838103245

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 103 KiloPascal
Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity