FDA UDI In Commercial Distribution 🇺🇸 United States

Aerogen® Solo Nebulizer System

DI: 05391517933239 · Model: 10-046 · AEROGEN LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aerogen® Solo Nebulizer System
Primary DI
05391517933239
Version / Model
10-046
Company Name
AEROGEN LIMITED
Labeler DUNS
989510003
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
8b490b9d-4f56-4a30-b58a-44093643d7fc

Device Description

Aerogen Solo Pediatric T-Piece

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
MR Unsafe
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
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
35457 Benchtop nebulizer, non-heated

Identifiers

Type ID
Primary 05391517933239

Customer Contacts

Phone
+35391540400

Premarket Submissions

Submission Number Supplement Number
K070642 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
450 – 1100 millibar
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius