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Connector, 1/4" X 1/2" W/Out Luer

FDA UDI

Class I (US FDA UDI)

by Novosci Corp.

Identity

Trade Name
CONNECTOR, 1/4" X 1/2" W/OUT LUER FDA UDI
Generic Name
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI
Device Name
A sterile plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension or shunt; it may also be used to connect ancillary disposable devices (e.g., temperature probe). It typically has a Y-shape or straight design and is profiled at its ends to create leak-proof connections. This is a single-use device. FDA UDI
Model / Reference
331024NS FDA UDI
Description
A sterile plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension or shunt; it may also be used to connect ancillary disposable devices (e.g., temperature probe). It typically has a Y-shape or straight design and is profiled at its ends to create leak-proof connections. This is a single-use device. FDA UDI

Identifiers

Catalog Number
331024NS FDA UDI
Primary DI / UDI-DI
B066331024NS1 FDA UDI
510(k) Number
K802542 FDA UDI
FDA Product Code
KRI FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4200 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Non-ISO80369-standardized small-bore linear connector, single-use

Connector, 1/4" X 1/2" W/Out Luer by Novosci Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-ISO80369-standardized small-bore linear connector, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novosci Corp.

Sources (1)

  • FDA UDI 656a9213-1f41-4449-8354-098f3a978c7f 36 fields · synced May 31, 2026