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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
Intravenous administration tubing extension set FDA UDI
Device Name
IV ADMINISTRATION SET, 92", VENTED SPIKE, DRIP CHAMBER, IN LINE FILTER, KEN_SEF SPLIT SEPTUM Y SITE, KEN_ROL ROTATING MALE LUER LOCK CONNECTOR, FLOW REGULATOR FDA UDI
Model / Reference
937025 FDA UDI
Description
IV ADMINISTRATION SET, 92", VENTED SPIKE, DRIP CHAMBER, IN LINE FILTER, KEN_SEF SPLIT SEPTUM Y SITE, KEN_ROL ROTATING MALE LUER LOCK CONNECTOR, FLOW REGULATOR FDA UDI

Identifiers

Catalog Number
937025 FDA UDI
Primary DI / UDI-DI
00810003750037 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 — 92 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

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Manufacturer

Manufacturer
Kentron Health Care, Inc.

Sources (1)

  • FDA UDI 3e693ab7-3d3c-4c41-aada-35321dea871b 36 fields · synced Jun 8, 2026