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Niagara

FDA UDI

Class II (US FDA UDI)

by Medisafe Uk Limited

Identity

Trade Name
Niagara FDA UDI
Generic Name
Sterilizer/disinfector rack FDA UDI
Device Name
Xi Multi Basket and tubing is used with the InnoWave Pro and PCF Pro Sonic Irrigators FDA UDI
Model / Reference
MP21906 FDA UDI
Description
Xi Multi Basket and tubing is used with the InnoWave Pro and PCF Pro Sonic Irrigators FDA UDI

Identifiers

Catalog Number
IW1051 FDA UDI
Primary DI / UDI-DI
05060247265230 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Sterilizer/disinfector rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6992 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sterilizer/disinfector rack

Niagara by Medisafe Uk Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilizer/disinfector rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medisafe Uk Limited

Sources (1)

  • FDA UDI 18abfaba-53d4-4d35-8ae1-9bd00d7277a5 35 fields · synced Jun 1, 2026