FDA UDI In Commercial Distribution 🇺🇸 United States

MAXFLO2

DI: 00817770020806 · Model: R223P08 · MAXTEC, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAXFLO2
Primary DI
00817770020806
Version / Model
R223P08
Company Name
MAXTEC, LLC
Labeler DUNS
169911828
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-27
Public Version
4
Public Version Date
2019-01-14
Public Version Status
Update
Public Device Record Key
ee0bc4ab-605b-4419-b465-e25c53293898

Device Description

MaxFlo2 Mini 0-70 LPM

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
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
BZR Mixer, Breathing Gases, Anesthesia Inhalation

GMDN Terms

Code Name
44225 Oxygen/air breathing gas mixer, hospital

Identifiers

Type ID
Primary 00817770020806

Premarket Submissions

Submission Number Supplement Number
K113232 000