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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Urine transfer IVD, sterile FDA UDI
Device Name
Specimen Container for Pneumatic Tube Systems 120 mL (4 oz.) Screw Cap Sterile FDA UDI
Model / Reference
16-9542 FDA UDI
Description
Specimen Container for Pneumatic Tube Systems 120 mL (4 oz.) Screw Cap Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
20612479197521 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Urine transfer IVD, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

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

No

FDA UDI

Category: Urine transfer IVD, sterile

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

Similar devices

Also classified as Urine transfer IVD, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI eb76b71a-4651-470c-af66-f919bce4733f 33 fields · synced May 30, 2026