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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
Stockinette FDA UDI
Device Name
Stockinette STERILE | BIAS CUT COTTON | SINGLE PLY 6 in. x 4 yds. FDA UDI
Model / Reference
16-3B-64 FDA UDI
Description
Stockinette STERILE | BIAS CUT COTTON | SINGLE PLY 6 in. x 4 yds. FDA UDI

Identifiers

Primary DI / UDI-DI
20612479123582 FDA UDI
FDA Product Code
IPM FDA UDI
GMDN Term
Stockinette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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 I — 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 3111be54-2fbe-4a26-aab4-794dafea2788 33 fields · synced May 30, 2026