Identity
- Trade Name
- Red Dot™ FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- 3M™ Red Dot™ Large Pre-Wired Monitoring Electrode 2289T, 3/POUCH;100POUCHES/CASE FDA UDI
- Model / Reference
- 2289T FDA UDI
- Description
- 3M™ Red Dot™ Large Pre-Wired Monitoring Electrode 2289T, 3/POUCH;100POUCHES/CASE FDA UDI
Identifiers
- Catalog Number
- 2289T FDA UDI
- Primary DI / UDI-DI
- 10707387762039 FDA UDI
- FDA Product Code
- DRX FDA UDI
- GMDN Term
- Electrocardiographic electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2360 FDA UDI
- 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrocardiographic electrode, single-use
Red Dot™ by 3m Company — 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
- 3m Company
Sources (1)
- FDA UDI 5e484f9f-0d1f-4edd-94ca-768627d137ae 35 fields · synced May 31, 2026