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PREMIXSLIP (4.2oz/125ml with mister)

FDA UDI

Class I (US FDA UDI)

by Ruhof Corporation

Identity

Trade Name
PREMIXSLIP (4.2oz/125ml with mister) FDA UDI
Generic Name
Surgical instrument maintenance lubricant FDA UDI
Device Name
Lubricant for medical Instrument FDA UDI
Model / Reference
34552-09 FDA UDI
Description
Lubricant for medical Instrument FDA UDI

Identifiers

Primary DI / UDI-DI
00810929010352 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Surgical instrument maintenance lubricant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 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

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: Surgical instrument maintenance lubricant

PREMIXSLIP (4.2oz/125ml with mister) by Ruhof Corporation — Class I — 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

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Manufacturer

Manufacturer
Ruhof Corporation

Sources (1)

  • FDA UDI 3fa47c03-549e-4e07-a63e-a9167b0f2fe1 34 fields · synced May 31, 2026