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Hako-Med
FDA UDIClass II (US FDA UDI)
by HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H.
Identity
- Trade Name
- Hako-Med FDA UDI
- Generic Name
- Interferential electrical stimulation system FDA UDI
- Model / Reference
- ElecDT FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260653010023 FDA UDI
- FDA Product Code
- IPF FDA UDILIH FDA UDI
- GMDN Term
- Interferential electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5850 FDA UDI882.5890 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Interferential electrical stimulation system
Hako-Med by HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H. — Class II — FDA UDI — listed in FDA GUDID
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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
Sources (1)
- FDA UDI fae7cf6e-a39d-40c8-bf97-065468478f5a 32 fields · synced May 30, 2026