← Back to catalogue

KC 18901-K Elbow Connector

FDA UDI

Class I (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name
KC 18901-K Elbow Connector FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
90 degree Elbow Connector - 15mm ID/22mm OD x15mm OD. Molded of polystyrene butadiene. Single patient use. FDA UDI
Model / Reference
KC 18901-K FDA UDI
Description
90 degree Elbow Connector - 15mm ID/22mm OD x15mm OD. Molded of polystyrene butadiene. Single patient use. FDA UDI

Identifiers

Catalog Number
KC 18901-K FDA UDI
Primary DI / UDI-DI
M996KC18901K0 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

No

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 18901-K Elbow Connector 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

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

Manufacturer

Sources (1)

  • FDA UDI 6d6e1a1c-4fc6-4de2-a2e6-f747e40be9e1 35 fields · synced Jun 8, 2026