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Connector, Adapter Needle Luer

FDA UDI

Class II (US FDA UDI)

by Novosci Corp.

Identity

Trade Name
CONNECTOR, ADAPTER NEEDLE LUER FDA UDI
Generic Name
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI
Device Name
A non-sterile device designed to connect together two or more tubes typically with the intention of creating an extension. The connecting ends of this device will typically be serrated to provide a secure grip for the applied tubes. Clips or other forms of locking devices may be applied over the tubes to further secure the fitting. This device will not be appropriate for connecting tubes that are designed to carry (withstand) high pressures [e.g., high pressure gases]. This is a single-use device. FDA UDI
Model / Reference
102357NS FDA UDI
Description
A non-sterile device designed to connect together two or more tubes typically with the intention of creating an extension. The connecting ends of this device will typically be serrated to provide a secure grip for the applied tubes. Clips or other forms of locking devices may be applied over the tubes to further secure the fitting. This device will not be appropriate for connecting tubes that are designed to carry (withstand) high pressures [e.g., high pressure gases]. This is a single-use device. FDA UDI

Identifiers

Catalog Number
102357NS FDA UDI
Primary DI / UDI-DI
B066102357NS1 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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

Yes

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, Adapter Needle Luer by Novosci Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novosci Corp.

Sources (1)

  • FDA UDI d88cf532-0058-48f8-8a07-c421d16dd337 35 fields · synced May 31, 2026