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KC 2126 Reducing Adapter

FDA UDI

Class I (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name
KC 2126 Reducing Adapter FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
Reducing adapter for use in breathing/ventilator circuit. 22mm ID x 22mm OD. Molded of polystyrene butadiene. Single Patient Use. FDA UDI
Model / Reference
KC 2126 FDA UDI
Description
Reducing adapter for use in breathing/ventilator circuit. 22mm ID x 22mm OD. Molded of polystyrene butadiene. Single Patient Use. FDA UDI

Identifiers

Catalog Number
KC 2126 FDA UDI
Primary DI / UDI-DI
M996KC21260 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Straight/elbow breathing circuit connector, single-use

KC 2126 Reducing Adapter by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Straight/elbow breathing circuit connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Instrumentation Industries, Incorporated

Sources (1)

  • FDA UDI a04ba811-fa66-4b18-9861-753f53ef6e9a 35 fields · synced May 31, 2026