FDA UDI In Commercial Distribution 🇺🇸 United States

Solaris

DI: 06900234100085 · Model: T200A-090101 · Solaris Medical Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
6
Pkg Device Count
1

Basic Information

Brand Name
Solaris
Primary DI
06900234100085
Version / Model
T200A-090101
Company Name
Solaris Medical Technology, Inc.
Labeler DUNS
527945351
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-24
Public Version
5
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
644f68d8-4232-4acf-8dcb-eb84c5a4fd29

Device Description

BCI Compatible Adult SpO2 Soft-Finger Sensor (0.9m cable)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
DQA Oximeter

GMDN Terms

Code Name
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Package 56900234100080
Primary 06900234100085
Package 46900234100083
Package 36900234100086
Package 26900234100089
Package 16900234100082

Premarket Submissions

Submission Number Supplement Number
K100077 000