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Pharmaceutical Innovations

FDA UDI

Class I (US FDA UDI)

by Pharmaceutical Innovations, Inc.

Identity

Trade Name
Pharmaceutical Innovations FDA UDI
Generic Name
General-body orifice lubricant, non-sterile FDA UDI
Device Name
Gentle Gel Lubricating Gel: 90 ml tube FDA UDI
Model / Reference
Gentle Gel Lubricating Gel FDA UDI
Description
Gentle Gel Lubricating Gel: 90 ml tube FDA UDI

Identifiers

Catalog Number
36-1500-90 FDA UDI
Primary DI / UDI-DI
00300361500905 FDA UDI
FDA Product Code
MMS FDA UDI
GMDN Term
General-body orifice lubricant, non-sterile 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

No

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

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: General-body orifice lubricant, non-sterile

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

Similar devices

Also classified as General-body orifice lubricant, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87eca648-6a6f-4a03-bb2f-7b1bb4e7cb05 35 fields · synced May 30, 2026