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Cidex

FDA UDI

Class II (US FDA UDI)

by Advanced Sterilization Products Services Inc.

Identity

Trade Name
Cidex FDA UDI
Generic Name
Medical device disinfection agent FDA UDI
Device Name
Cidex Activated Dialdehyde 4.7 Liter FDA UDI
Model / Reference
2266 FDA UDI
Description
Cidex Activated Dialdehyde 4.7 Liter FDA UDI

Identifiers

Catalog Number
2266 FDA UDI
Primary DI / UDI-DI
10705037044580 FDA UDI
510(k) Number
K060618 FDA UDI
FDA Product Code
MED FDA UDI
GMDN Term
Medical device disinfection agent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6885 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

Yes

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

No

FDA UDI

Category: Medical device disinfection agentGlutaraldehyde device disinfectant/sterilant test strip

Cidex by Advanced Sterilization Products Services Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glutaraldehyde device disinfectant/sterilant test strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Sterilization Products Services Inc.

Sources (1)

  • FDA UDI 69e1d42f-4e83-4237-9a85-f51e8eec5703 37 fields · synced May 30, 2026