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Teknobios

FDA UDI

Class I (US FDA UDI)

by Amil Care Corporation

Identity

Trade Name
Teknobios FDA UDI
Generic Name
Airborne device-disinfectant diffuser FDA UDI
Device Name
Diffuser of ready-to-use liquid solutions FDA UDI
Model / Reference
1L-2L-5L (hub) FDA UDI
Description
Diffuser of ready-to-use liquid solutions FDA UDI

Identifiers

Catalog Number
2023.t FDA UDI
Primary DI / UDI-DI
G0602023T0 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Airborne device-disinfectant diffuser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Airborne device-disinfectant diffuser

Teknobios by Amil Care Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airborne device-disinfectant diffuser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d252f2a8-8cc7-46a7-90df-a8775486bed1 34 fields · synced May 30, 2026