FDA UDI Not in Commercial Distribution 🇺🇸 United States

MAXO2+

DI: 00817770020677 · Model: R217P62-004 · MAXTEC, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAXO2+
Primary DI
00817770020677
Version / Model
R217P62-004
Company Name
MAXTEC, LLC
Labeler DUNS
169911828
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
5
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
fccca43f-7f28-4c7e-95e0-c222c47f9d25
Distribution End Date
2019-05-06

Device Description

MaxO2+A Analyzer with Adapter

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
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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

GMDN Terms

Code Name
35219 Respiratory oxygen monitor, line-powered

Identifiers

Type ID
Primary 00817770020677

Premarket Submissions

Submission Number Supplement Number
K040484 000