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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
B15088815731214 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nurse Assist, Inc.

Sources (1)

  • FDA UDI 8626a6bb-19bf-40cd-9095-32fdacec4546 33 fields · synced May 30, 2026