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Tonowash

FDA UDI

Class II (US FDA UDI)

by Eye-Novation LLC

Identity

Trade Name
Tonowash FDA UDI
Generic Name
Medical device disinfection solution container FDA UDI
Device Name
Device for automatically disinfecting tonometer tips FDA UDI
Model / Reference
1.0 FDA UDI
Description
Device for automatically disinfecting tonometer tips FDA UDI

Identifiers

Primary DI / UDI-DI
00860012823505 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Medical device disinfection solution container 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

Yes

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

No

FDA UDI

Category: Medical device disinfection solution container

Tonowash by Eye-Novation LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device disinfection solution container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eye-Novation LLC

Sources (1)

  • FDA UDI 4abd9b3e-cdb0-4c31-a6f6-2c65f9ba583c 33 fields · synced Jun 6, 2026