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Flex Surgical Instrument Washer

FDA UDI

Class II (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Flex Surgical Instrument Washer FDA UDI
Generic Name
Surgical instrument washer/disinfector (chemical/thermal) FDA UDI
Device Name
Flex Surgical Instrument Washer FDA UDI
Model / Reference
CS-0040-000 FDA UDI
Description
Flex Surgical Instrument Washer FDA UDI

Identifiers

Catalog Number
CS-0040-000 FDA UDI
Primary DI / UDI-DI
10841736111663 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Surgical instrument washer/disinfector (chemical/thermal) 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical instrument washer/disinfector (chemical/thermal)

Flex Surgical Instrument Washer by Skytron, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument washer/disinfector (chemical/thermal).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 5fa07228-58b7-404a-a5e1-853d5072bfb1 35 fields · synced May 30, 2026