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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Peripheral intravenous cannula FDA UDI
Device Name
Sliding Safety IV Catheter STRAIGH HUB 20G x 1 in (1.1 mm x 25.4 mm) FDA UDI
Model / Reference
200-IVS201 FDA UDI
Description
Sliding Safety IV Catheter STRAIGH HUB 20G x 1 in (1.1 mm x 25.4 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
10612479267487 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral intravenous cannula 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peripheral intravenous cannula

McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 459e6886-a289-48aa-a3a5-b54665609497 33 fields · synced May 30, 2026