FDA UDI In Commercial Distribution 🇺🇸 United States

FL9000

DI: 05055931111009 · Model: FL9000-04U · FLEXICARE MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
FL9000
Primary DI
05055931111009
Version / Model
FL9000-04U
Company Name
FLEXICARE MEDICAL LIMITED
Labeler DUNS
504406273
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-14
Public Version
1
Public Version Date
2024-03-22
Public Version Status
New
Public Device Record Key
753e27de-6b77-473b-bd0b-b3741d2b6ec8

Device Description

Respiratory Humidifier Single Use Temperature Probe

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

GMDN Terms

Code Name
12050 Heated respiratory humidifier

Identifiers

Type ID
Primary 05055931111009

Premarket Submissions

Submission Number Supplement Number
K161314 000