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Jetox

FDA UDI

Class II (US FDA UDI)

by Tav - Tech Ltd

Identity

Trade Name
Jetox FDA UDI
Generic Name
Pressure-regulated wound irrigation solution applicator, pneumatic FDA UDI
Model / Reference
Jetox tubing FDA UDI

Identifiers

Catalog Number
JNO-013 FDA UDI
Primary DI / UDI-DI
07290014242265 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Pressure-regulated wound irrigation solution applicator, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure-regulated wound irrigation solution applicator, pneumatic

Jetox by Tav - Tech Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure-regulated wound irrigation solution applicator, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tav - Tech Ltd

Sources (1)

  • FDA UDI 70199262-3cb2-463a-b9d8-797eed829cee 34 fields · synced May 30, 2026