Covidien

FDA UDI

Class II (US FDA UDI)

by Nurse Assist, Inc.

Identity

Trade Name: COVIDIEN FDA UDI
Generic Name: Vascular catheter flush syringe FDA UDI
Model / Reference: 8881573121 FDA UDI

Identifiers

Primary DI / UDI-DI: B15088815731212 FDA UDI
510(k) Number: K150143 FDA UDI
FDA Product Code: NGT FDA UDI
GMDN Term: Vascular catheter flush syringe FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Vascular catheter flush syringe

Covidien by Nurse Assist, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter flush syringe.

Excelsior — MEDLINE INDUSTRIES, INC. · Class II
Excelsior — MEDLINE INDUSTRIES, INC. · Class II
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Excelsior — MEDLINE INDUSTRIES, INC. · Class II
Centurion — Centurion Medical Products · Class II
Centurion — Centurion Medical Products · Class II
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Excelsior — MEDLINE INDUSTRIES, INC. · Class II

Cleared under the same submission

K150143 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Nurse Assist, Inc.

Sources (1)

FDA UDI 5d7b4594-0507-4f9b-977c-dcedd8a917aa 33 fields · synced May 30, 2026