FDA UDI Not in Commercial Distribution 🇺🇸 United States

FloSense

DI: B279DP2112 · Model: kushion klip · S D I DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
250

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Basic Information

Brand Name
FloSense
Primary DI
B279DP2112
Version / Model
kushion klip
Catalog Number
DP211-2
Company Name
S D I DIAGNOSTICS INC
Labeler DUNS
037690120
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
250
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2019-08-26
Public Version Status
Update
Public Device Record Key
de0c2ab4-6e9a-4f1f-859f-73bdb985a358
Distribution End Date
2019-07-31

Device Description

FloSense Sensor

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JAX Pneumotachometer

GMDN Terms

Code Name
35282 Pulmonary function analysis system, adult

Identifiers

Type ID
Primary B279DP2112
Unit of Use DP21123

Premarket Submissions

Submission Number Supplement Number
K990962 000