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ActivePure Medical Guardian

FDA UDI

Class II (US FDA UDI)

by Activepure Medical Llc

Identity

Trade Name
ActivePure Medical Guardian FDA UDI
Generic Name
High-efficiency filter air cleaner, mobile FDA UDI
Device Name
Medical Ultraviolet Air Purifier FDA UDI
Model / Reference
F170A FDA UDI
Description
Medical Ultraviolet Air Purifier FDA UDI

Identifiers

Primary DI / UDI-DI
00860006810108 FDA UDI
510(k) Number
K201220 FDA UDI
FDA Product Code
FRA FDA UDI
GMDN Term
High-efficiency filter air cleaner, mobile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6500 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

Yes

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: High-efficiency filter air cleaner, mobile

ActivePure Medical Guardian by Activepure Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as High-efficiency filter air cleaner, mobile.

Cleared under the same submission

K201220 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0ee7e50-f3f5-4dbb-adf2-537075a90b53 35 fields · synced May 30, 2026