← Back to catalogue

Timm Medical

FDA UDI

Class I (US FDA UDI)

by Parker Laboratories, Inc.

Identity

Trade Name
Timm Medical FDA UDI
Generic Name
General-body orifice lubricant FDA UDI
Device Name
Lubricating Gel 142 gram gel (5 oz) FDA UDI
Model / Reference
57-05-144738 FDA UDI
Description
Lubricating Gel 142 gram gel (5 oz) FDA UDI

Identifiers

Primary DI / UDI-DI
00855683006739 FDA UDI
510(k) Number
K864556 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-body orifice lubricant

Timm Medical by Parker Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-body orifice lubricant.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 261b2b62-4073-41e1-8541-7baa1e816de9 35 fields · synced May 30, 2026