← Back to catalogue

McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Multi-purpose surgical instrument lubricant FDA UDI
Device Name
Lubricating Jelly STERILE | WATER SOLUBLE | GREASELESS | UNSCENTED 4 oz. FDA UDI
Model / Reference
16-8919 FDA UDI
Description
Lubricating Jelly STERILE | WATER SOLUBLE | GREASELESS | UNSCENTED 4 oz. FDA UDI

Identifiers

Primary DI / UDI-DI
00612479225039 FDA UDI
FDA Product Code
KMJ FDA UDI
GMDN Term
Multi-purpose surgical instrument lubricant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6375 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose surgical instrument lubricant

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

Similar devices

Also classified as Multi-purpose surgical instrument lubricant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 46e6c4b6-bdef-4361-a2dc-ae5354879ec9 33 fields · synced Jun 1, 2026