Identity
- Trade Name
- OrthoCor Medical FDA UDI
- Generic Name
- Hand-held deep-tissue electromagnetic stimulator FDA UDI
- Device Name
- OrthoCor Pemf NOW is a lightweight, portable, portable pulsed electromagnetic field (Nonthermal Shortwave Diathermy) device designed for adjunctive use in the palliative treatment of post-operative pain and edema. FDA UDI
- Model / Reference
- Pemf NOW FDA UDI
- Description
- OrthoCor Pemf NOW is a lightweight, portable, portable pulsed electromagnetic field (Nonthermal Shortwave Diathermy) device designed for adjunctive use in the palliative treatment of post-operative pain and edema. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851979007282 FDA UDI
- FDA Product Code
- ILX FDA UDI
- GMDN Term
- Hand-held deep-tissue electromagnetic stimulator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5290 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Hand-held deep-tissue electromagnetic stimulator
OrthoCor Medical by Caerus Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Manufacturer
- Caerus Corporation
Sources (1)
- FDA UDI e37cb29b-9496-488e-8490-990175da7489 33 fields · synced May 30, 2026