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Rapicide Glutaraldehyde Indicator Test Strips

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Rapicide Glutaraldehyde Indicator Test Strips FDA UDI
Generic Name
Medical device disinfection solution test strip FDA UDI
Device Name
Rapicide Glutaraldehyde Indicator Test Strips FDA UDI
Model / Reference
ML02-0120 FDA UDI
Description
Rapicide Glutaraldehyde Indicator Test Strips FDA UDI

Identifiers

Catalog Number
ML020120 FDA UDI
Primary DI / UDI-DI
10677964063623 FDA UDI
510(k) Number
K080750 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Medical device disinfection solution test strip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

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 solution test strip

Rapicide Glutaraldehyde Indicator Test Strips by Medivators Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device disinfection solution test strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medivators Inc.

Sources (1)

  • FDA UDI a6c3e65e-f371-40b8-bce5-51564161aafa 36 fields · synced May 30, 2026