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Kenaflexx

FDA UDI

Class II (US FDA UDI)

by Kentron Health Care, Inc.

Identity

Trade Name
KENAFLEXX FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
I.V. ADMINISTRATION SET 10 DROPS 110" WITH 3 KEN_FLO CONNECTORS FDA UDI
Model / Reference
948537 FDA UDI
Description
I.V. ADMINISTRATION SET 10 DROPS 110" WITH 3 KEN_FLO CONNECTORS FDA UDI

Identifiers

Catalog Number
948537 FDA UDI
Primary DI / UDI-DI
00852244007266 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive 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 — 110 Inch FDA UDI

Category: Basic intravenous administration set, noninvasive

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

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kentron Health Care, Inc.

Sources (1)

  • FDA UDI 0f6944d1-17be-44d6-b140-3ff90829b395 36 fields · synced May 31, 2026