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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
Stockinette FDA UDI
Device Name
Stockinette STERILE | TUBULAR COTTON | DOUBLE PLY 6 in x 72 in FDA UDI
Model / Reference
16-3S-672 FDA UDI
Description
Stockinette STERILE | TUBULAR COTTON | DOUBLE PLY 6 in x 72 in FDA UDI

Identifiers

Primary DI / UDI-DI
20612479123735 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Stockinette FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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: Stockinette

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

Similar devices

Also classified as Stockinette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c16e27ee-e67a-427f-ba1e-f23fb767c741 33 fields · synced May 30, 2026