Identity
- Trade Name
- TECNIMED FDA UDI
- Generic Name
- Insect bite/sting electrical stimulator FDA UDI
- Device Name
- Limited output transcutaneous piezoelectric stimulator for skin reactions associated with insect bites. FDA UDI
- Model / Reference
- Disc-o-Click FDA UDI
- Description
- Limited output transcutaneous piezoelectric stimulator for skin reactions associated with insect bites. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00182097000368 FDA UDI
- FDA Product Code
- OSG FDA UDI
- GMDN Term
- Insect bite/sting electrical stimulator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5894 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Insect bite/sting electrical stimulator
Tecnimed by Tecnimed Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Insect bite/sting electrical stimulator.
- mibest — Beijing Choice Electronic Technology Co., Ltd. · Class II
- Walgreens — WALGREEN CO. · Class II
- Tecnibrands — TECNIMED SRL · Class II
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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Tecnimed Srl
Sources (1)
- FDA UDI eaf07fc9-8112-4c05-87f0-1f617ea52f3c 34 fields · synced Jun 6, 2026