← Back to catalogue

Actril Indicator Test Strips

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Actril Indicator Test Strips FDA UDI
Generic Name
Organic peroxy acid device sterilant, single-use FDA UDI
Model / Reference
78280-000 FDA UDI

Identifiers

Primary DI / UDI-DI
10677964105972 FDA UDI
510(k) Number
K861730 FDA UDI
FDA Product Code
FKQ FDA UDI
GMDN Term
Organic peroxy acid device sterilant, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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: Organic peroxy acid device sterilant, single-use

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

Similar devices

Also classified as Organic peroxy acid device sterilant, single-use.

Cleared under the same submission

K861730 also covers:

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
Medivators Inc.

Sources (1)

  • FDA UDI adcd3d92-88f6-49d1-93df-02598fdbdde3 33 fields · synced May 29, 2026