Identity
- Trade Name
- Nova Plus® FDA UDI
- Generic Name
- Electrosurgical return electrode, single-use FDA UDI
- Device Name
- 3M™ Patient Plate, Corded, Split, Large, 40 per Case, 7179V FDA UDI
- Model / Reference
- 7179V FDA UDI
- Description
- 3M™ Patient Plate, Corded, Split, Large, 40 per Case, 7179V FDA UDI
Identifiers
- Catalog Number
- 7179V FDA UDI
- Primary DI / UDI-DI
- 50707387454628 FDA UDI
- 510(k) Number
- K833364 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrosurgical return electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Nova Plus® by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K833364 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI dba0d892-7aa5-4c9a-a0c8-d9cbc5870158 37 fields · synced May 31, 2026