← Back to catalogue

Kenaflexx

FDA UDI

Class II (US FDA UDI)

by Kentron Health Care, Inc.

Identity

Trade Name
KENAFLEXX FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
12" IV EXTENSIO SET WITH FEMALE LUER CONNECTOR, KENTRON GRAVITO FLOW CONTROLLER, ONE KEN_FLO Y SITE, SLIDING CLAMP, KEN_ROL MALE ROTATING LUER LOCK CONNECTOR. FDA UDI
Model / Reference
940013 FDA UDI
Description
12" IV EXTENSIO SET WITH FEMALE LUER CONNECTOR, KENTRON GRAVITO FLOW CONTROLLER, ONE KEN_FLO Y SITE, SLIDING CLAMP, KEN_ROL MALE ROTATING LUER LOCK CONNECTOR. FDA UDI

Identifiers

Catalog Number
940013 FDA UDI
Primary DI / UDI-DI
00810003750082 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 12 Inch FDA UDI

Category: Intravenous administration tubing extension set

Kenaflexx by Kentron Health Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Kentron Health Care, Inc.

Sources (1)

  • FDA UDI c6405147-562c-4e27-ae2e-335254cd10e7 35 fields · synced Jun 8, 2026