FDA UDI In Commercial Distribution 🇺🇸 United States

MAX02 ME

DI: 00853061006302 · Model: R230P01-001 · MAXTEC, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAX02 ME
Primary DI
00853061006302
Version / Model
R230P01-001
Company Name
MAXTEC, LLC
Labeler DUNS
169911828
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2019-01-15
Public Version Status
Update
Public Device Record Key
f1529e45-9cb5-421e-bcbc-4507447c1237

Device Description

International Analyzer

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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

GMDN Terms

Code Name
46049 Respiratory oxygen monitor, battery-powered

Identifiers

Type ID
Primary 00853061006302

Premarket Submissions

Submission Number Supplement Number
K153659 000