← Back to catalogue

Minncare HD

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Minncare HD FDA UDI
Generic Name
Organic peroxy acid device sterilant, single-use FDA UDI
Device Name
Minncare HD (4 x 1 Gallon) FDA UDI
Model / Reference
3029764 FDA UDI
Description
Minncare HD (4 x 1 Gallon) FDA UDI

Identifiers

Catalog Number
3029764 FDA UDI
Primary DI / UDI-DI
00724995223298 FDA UDI
510(k) Number
K133724 FDA UDI
FDA Product Code
NIH FDA UDI
GMDN Term
Organic peroxy acid device sterilant, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5665 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Organic peroxy acid device sterilant, single-use

Minncare HD 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

K133724 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 dfb549cb-b6e6-4ab7-a4ea-b00aade04339 37 fields · synced Jun 8, 2026