Identity
- Trade Name
- ATTRACT™ FDA UDI
- Generic Name
- Head-worn bone-conduction hearing aid holder, reusable FDA UDI
- Device Name
- BASE PLATE S0266-02 2 DOT BLACK FDA UDI
- Model / Reference
- S0266-02 FDA UDI
- Description
- BASE PLATE S0266-02 2 DOT BLACK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00643169719569 FDA UDI
- 510(k) Number
- K153391 FDA UDI
- FDA Product Code
- LXB FDA UDI
- GMDN Term
- Head-worn bone-conduction hearing aid holder, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3302 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Attract™ by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI 045bfcd2-d97c-4b5f-a6b0-a0f1c71701dc 36 fields · synced May 31, 2026