FDA UDI In Commercial Distribution 🇺🇸 United States

KENAFLEXX

DI: 00810003750075 · Model: 940012 · KENTRON HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KENAFLEXX
Primary DI
00810003750075
Version / Model
940012
Catalog Number
940012
Company Name
KENTRON HEALTHCARE, INC.
Labeler DUNS
618825723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-18
Public Version
1
Public Version Date
2018-12-19
Public Version Status
New
Public Device Record Key
8c18a130-7cb1-4f45-9573-e15560a6fef5

Device Description

12" IV EXTENSION SET WITH FEMALE LUER, KENTRON GRAVITO FLOW REGULATOR, ONE KEN_SEF SPLIT SEPTUM Y SITE, SLIDING CLAMP, KEN_ROL ROTATING MALE LUER LOCK CONNECTOR.

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 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
LHI Set, I.V. Fluid Transfer

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 10810003750072
Primary 00810003750075

Customer Contacts

Phone
615-384-0573

Device Sizes

Type Value Unit Text
Length 12 Inch