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
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Also classified as Drug-delivery iontophoresis patch.
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- PERFORMA — Performance Health Supply, LLC · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
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Manufacturer
- Manufacturer
- LTS Therapy Systems, LLC
Sources (1)
- FDA UDI a51029e3-dabe-4068-9dda-00b1b209bf8d 35 fields · synced May 30, 2026