Identity
- Trade Name
- Mammosite Multi-lumen Applicator Tray FDA UDI
- Generic Name
- Breast brachytherapy system applicator, remote-afterloading FDA UDI
- Device Name
- MAMMOSITE MULTI-LUMEN 3.5-5.0 CM APPLICATOR used to position tissue and the radioactive source during breast brachytherapy treatments. FDA UDI
- Model / Reference
- ML2345 FDA UDI
- Description
- MAMMOSITE MULTI-LUMEN 3.5-5.0 CM APPLICATOR used to position tissue and the radioactive source during breast brachytherapy treatments. FDA UDI
Identifiers
- Catalog Number
- ML2345 FDA UDI
- Primary DI / UDI-DI
- 15420045505025 FDA UDI
- 510(k) Number
- K092405 FDA UDI
- FDA Product Code
- JAQ FDA UDI
- GMDN Term
- Breast brachytherapy system applicator, remote-afterloading FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.5700 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Mammosite Multi-lumen Applicator Tray by Hologic, 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
- Hologic, Inc.
Sources (1)
- FDA UDI 6d31bad1-fdeb-4c54-91b3-476c1d51748c 37 fields · synced May 30, 2026