FDA UDI In Commercial Distribution 🇺🇸 United States

KENOREX

DI: 00851785007582 · Model: 919960 · KENTRON HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
KENOREX
Primary DI
00851785007582
Version / Model
919960
Catalog Number
919960
Company Name
KENTRON HEALTHCARE, INC.
Labeler DUNS
618825723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
bc783665-a31e-4db4-9c5c-e48dab2c4cb3

Device Description

ENDOTRACHEAL TUBE CUFFED 6.0 MM WITH SUCTION PORT MURPHY EYE

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BTR Tube, Tracheal (W/Wo Connector)

GMDN Terms

Code Name
46967 Basic endotracheal tube, single-use

Identifiers

Type ID
Primary 00851785007582
Package 10851785007589
Package 20851785007589

Customer Contacts

Phone
615-384-0573

Premarket Submissions

Submission Number Supplement Number
K110269 000