FDA UDI In Commercial Distribution 🇺🇸 United States

KENOREX

DI: 10852244007362 · Model: 779504 · KENTRON HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KENOREX
Primary DI
10852244007362
Version / Model
779504
Catalog Number
779504
Company Name
KENTRON HEALTHCARE, INC.
Labeler DUNS
618825723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9790c7e0-e735-4cd5-905c-5fecd8918519

Device Description

RESUSCITATOR MANOMETER 0-60 CMS WATER 30 MM ID

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

GMDN Terms

Code Name
46634 Airway pressure monitor, non-powered

Identifiers

Type ID
Package 00852244007365
Primary 10852244007362

Customer Contacts

Phone
615-384-0573

Premarket Submissions

Submission Number Supplement Number
K140370 000