Identity

Trade Name
Travanti FDA UDI
Generic Name
Drug-delivery iontophoresis patch FDA UDI
Device Name
This kit contains two (2) devices: 1) IontoPatch: Primary DI Number, 10815611020005 2) Saline: Primary DI Number, 04026704396047 The IontoPatch is single use and disposable. The patch is used in conjunction with the saline. FDA UDI
Model / Reference
STAT FDA UDI
Description
This kit contains two (2) devices: 1) IontoPatch: Primary DI Number, 10815611020005 2) Saline: Primary DI Number, 04026704396047 The IontoPatch is single use and disposable. The patch is used in conjunction with the saline. FDA UDI

Identifiers

Primary DI / UDI-DI
20815611021009 FDA UDI
510(k) Number
K992708 FDA UDI
GMDN Term
Drug-delivery iontophoresis patch FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Drug-delivery iontophoresis patch

Travanti by LTS Therapy Systems, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Drug-delivery iontophoresis patch.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a51029e3-dabe-4068-9dda-00b1b209bf8d 35 fields · synced May 30, 2026