FDA UDI In Commercial Distribution 🇺🇸 United States

IRMA™ AX+

DI: 07350046131736 · Model: 4768 · Masimo Sweden AB
Product Codes
7
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IRMA™ AX+
Primary DI
07350046131736
Version / Model
4768
Catalog Number
4768
Company Name
Masimo Sweden AB
Labeler DUNS
632369067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-11
Public Version
5
Public Version Date
2023-07-20
Public Version Status
Update
Public Device Record Key
6bf68411-1344-4592-b4c5-42c3127a3f82

Device Description

IRMA™ AX+

Device Characteristics

Single Use
No
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
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
CBS Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)
CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)
CBR Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.)
NHP Analyzer, Gas, Sevoflurane, Gaseous-Phase (Anesthetic Concentration)
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
NHQ Analyzer, Gas, Isoflurane, Gaseous-Phase (Anesthetic Concentration)
NHO Analyzer, Gas, Desflurane, Gaseous-Phase (Anesthetic Concentration)

GMDN Terms

Code Name
37061 Patient monitoring system module, multiple-gas

Identifiers

Type ID
Primary 07350046131736