← Back to catalogue

The Pyure Company

FDA UDI

Class II (US FDA UDI)

by The Pyure Company Inc

Identity

Trade Name
The Pyure Company FDA UDI
Generic Name
Ultraviolet-activated air cleaner FDA UDI
Device Name
Medical Ultraviolet Air Cleaner FDA UDI
Model / Reference
MDU/RX FDA UDI
Description
Medical Ultraviolet Air Cleaner FDA UDI

Identifiers

Catalog Number
00819355020218 FDA UDI
Primary DI / UDI-DI
00819355020218 FDA UDI
510(k) Number
K133800 FDA UDI
FDA Product Code
FRA FDA UDI
GMDN Term
Ultraviolet-activated air cleaner 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

No

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

Yes

FDA UDI

Category: Ultraviolet-activated air cleaner

The Pyure Company by The Pyure Company Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet-activated air cleaner.

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
The Pyure Company Inc

Sources (1)

  • FDA UDI f77a3f29-903a-41a7-8d48-2b9e79cb106e 36 fields · synced May 30, 2026