FDA UDI In Commercial Distribution 🇺🇸 United States

EZflow MAX

DI: 10641043320099 · Model: 10-32009 · MERCURY ENTERPRISES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EZflow MAX
Primary DI
10641043320099
Version / Model
10-32009
Company Name
MERCURY ENTERPRISES, INC.
Labeler DUNS
032705659
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-09
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
cd738e55-abcb-41ec-8dc7-252e2e878baa

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
Yes
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
Yes
Has Expiration Date
Yes
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
Package 30641043320093
Primary 10641043320099

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K993558 000