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InnoWave

FDA UDI

Class II (US FDA UDI)

by Medisafe Uk Limited

Identity

Trade Name
InnoWave FDA UDI
Generic Name
Sterilizer/disinfector rack FDA UDI
Device Name
The Standard Basket for SI SA is used with the Medisafe SISA. FDA UDI
Model / Reference
IW1010 FDA UDI
Description
The Standard Basket for SI SA is used with the Medisafe SISA. FDA UDI

Identifiers

Catalog Number
IW1010 FDA UDI
Primary DI / UDI-DI
00724995152826 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

InnoWave 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 0897e6e9-2e22-4736-b4e3-a12ea3a68d39 35 fields · synced May 30, 2026