FDA UDI In Commercial Distribution 🇺🇸 United States

SpO2 Sensor

DI: 00884838010239 · Model: Reusable SpO2 Sensor Adult · Philips Medizin Systeme Böblingen GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpO2 Sensor
Primary DI
00884838010239
Version / Model
Reusable SpO2 Sensor Adult
Catalog Number
989803128591
Company Name
Philips Medizin Systeme Böblingen GmbH
Labeler DUNS
314101143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-21
Public Version
8
Public Version Date
2023-05-04
Public Version Status
Update
Public Device Record Key
71342f94-62cd-460e-854e-33f7f87b4235

Device Description

Reusable SpO2 Sensor Adult

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
DQA Oximeter

GMDN Terms

Code Name
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Primary 00884838010239

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-40 – 158 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
57 – 107.5 KiloPascal