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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
General-body orifice lubricant FDA UDI
Device Name
JELLY, LUBE, STERILE, FOIL PACK, 5G FDA UDI
Model / Reference
MDS032280 FDA UDI
Description
JELLY, LUBE, STERILE, FOIL PACK, 5G FDA UDI

Identifiers

Catalog Number
MDS032280 FDA UDI
Primary DI / UDI-DI
30080196291575 FDA UDI
FDA Product Code
KMJ FDA UDI
GMDN Term
General-body orifice 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

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

No

FDA UDI

Category: General-body orifice lubricant

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-body orifice lubricant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30c1b2bc-5045-48fb-87f7-a54fd4a62a3b 35 fields · synced May 30, 2026