Pediatric Tubing Organizrer - Non-Sterile

FDA UDI

Class I (US FDA UDI)

by Novosci Corp.

Identity

Trade Name: PEDIATRIC TUBING ORGANIZRER - 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: 311034NS 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: 311034NS FDA UDI
Primary DI / UDI-DI: B066311034NS1 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: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Novosci Corp.

Sources (1)

FDA UDI f7c61d22-2d9e-4e84-b060-0b506b667cf8 36 fields · synced May 30, 2026