FDA UDI In Commercial Distribution 🇺🇸 United States

NuFLO2 Hyperinflation System

DI: 10641043568019 · Model: 10-56801 · MERCURY ENTERPRISES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NuFLO2 Hyperinflation System
Primary DI
10641043568019
Version / Model
10-56801
Company Name
MERCURY ENTERPRISES, INC.
Labeler DUNS
032705659
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
e4fb7471-37b7-4795-9ec9-3ec9faa0e016

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
MR Conditional
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
NHK Resuscitator,Manual,Non Self-Inflating

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 30641043568013
Primary 10641043568019

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K001714 000