Identity
- Trade Name
- E-A-RTONE™ FDA UDI
- Generic Name
- Earphone, insert FDA UDI
- Device Name
- 3M(TM) E-A-RTONE(TM) Insert Earphone 3A 50 ohm Original Equipment Manufacturer model 410-3013, 1/case FDA UDI
- Model / Reference
- 410-3013 FDA UDI
- Description
- 3M(TM) E-A-RTONE(TM) Insert Earphone 3A 50 ohm Original Equipment Manufacturer model 410-3013, 1/case FDA UDI
Identifiers
- Catalog Number
- 410-3013 FDA UDI
- Primary DI / UDI-DI
- 00080529191212 FDA UDI
- FDA Product Code
- EWO FDA UDI
- GMDN Term
- Earphone, insert FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.1050 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Earphone, insert
E-A-Rtone™ 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 b7dba32c-980a-4a14-a6e3-4ad14667ba30 35 fields · synced May 30, 2026