← Back to catalogue

Skytron Lubricant

FDA UDI

Class II (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron Lubricant FDA UDI
Generic Name
Surgical instrument maintenance lubricant FDA UDI
Device Name
Skytron Lubricant, QTY 2, 2.5 gallon containers FDA UDI
Model / Reference
J5-010-32 FDA UDI
Description
Skytron Lubricant, QTY 2, 2.5 gallon containers FDA UDI

Identifiers

Catalog Number
J5-010-32 FDA UDI
Primary DI / UDI-DI
10841736110833 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Surgical instrument maintenance lubricant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6992 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument maintenance lubricant

Skytron Lubricant by Skytron, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument maintenance 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
Skytron, LLC

Sources (1)

  • FDA UDI 37072380-dc75-48cd-9997-07bd20d77a3b 34 fields · synced May 31, 2026