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Tubing Organizer - Non-Sterile

FDA UDI

Class I (US FDA UDI)

by Novosci Corp.

Identity

Trade Name
TUBING ORGANIZER - NON-STERILE FDA UDI
Generic Name
Medical/surgical interventional tube/cable securement clip, single-use FDA UDI
Device Name
A small, non-sterile device with a locking/holding mechanism designed to secure most any kind of tubing or tubing-like device (e.g., cables, cords) to a patient or to a surgical drape during a clinical intervention. It is typically designed as: 1) an adhesive pad (plaster), strip, or bandage intended to attach to the patient's skin or drape with the exposed side (top side) having an integrated fixation mechanism (e.g., Velcro hook/loop closure); or 2) a mechanical closure or gripping system intended to hold the tubing or tubing hub in place. This device is not designed to hold a specific type or brand of tubing. This is a single-use device intended to be sterilized prior to use. FDA UDI
Model / Reference
311033NS FDA UDI
Description
A small, non-sterile device with a locking/holding mechanism designed to secure most any kind of tubing or tubing-like device (e.g., cables, cords) to a patient or to a surgical drape during a clinical intervention. It is typically designed as: 1) an adhesive pad (plaster), strip, or bandage intended to attach to the patient's skin or drape with the exposed side (top side) having an integrated fixation mechanism (e.g., Velcro hook/loop closure); or 2) a mechanical closure or gripping system intended to hold the tubing or tubing hub in place. This device is not designed to hold a specific type or brand of tubing. This is a single-use device intended to be sterilized prior to use. FDA UDI

Identifiers

Catalog Number
311033NS FDA UDI
Primary DI / UDI-DI
B066311033NS1 FDA UDI
FDA Product Code
KRI FDA UDI
GMDN Term
Medical/surgical interventional tube/cable securement clip, 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

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: Medical/surgical interventional tube/cable securement clip, single-use

Tubing Organizer - Non-Sterile by Novosci Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical/surgical interventional tube/cable securement clip, 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 c6f4e25c-8d70-4899-8c71-439046e2660e 35 fields · synced May 30, 2026