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Sign in to claim this brandBARD BRACHYTHERAPY, INC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 295 E. LIES RD., CAROL STREAM, IL, 60188
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3002942387
- DUNS Number
- —
Catalogue (76)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TheraSeed® | TS200CN | FDA UDI | Class II | Active |
| QuickLink™ | 70310SGA2 | FDA UDI | Class I | Active |
| TheraSeed® | TS200LS | FDA UDI | Class II | Active |
| BrachySource™ | 1251PAPF | FDA UDI | Class II | Active |
| TheraSeed® | TS200CSA | FDA UDI | Class II | Active |
| BrachyStar™ | 718205 | FDA UDI | Class I | Active |
| BrachySource™ | 1251CSR | FDA UDI | Class II | Active |
| SourceLink™ | 7030310 | FDA UDI | Class II | Active |
| QuickLink™, SourceLink™ | 70301QC20 | FDA UDI | Class II | Active |
| BrachySource™ | PS1251L | FDA UDI | Class II | Active |
| BrachySource™ | PS1251C | FDA UDI | Class II | Active |
| BrachySource™ | PS1251K | FDA UDI | Class II | Active |
| TheraSeed®, SourceCap™ | 200PAPF | FDA UDI | Class II | Active |
| QuickLink™, BrachySource™ | 1251QLL | FDA UDI | Class II | Active |
| BrachySource™, ReadyLink™ | STM1251RL | FDA UDI | Class II | Active |
| QuickLink™, BrachySource™ | 1251QCS | FDA UDI | Class II | Active |
| SourceLink™ | 70308A1 | FDA UDI | Class I | Unknown |
| QuickLink™, TheraSeed® | 200QCS | FDA UDI | Class II | Active |
| TheraSeed® | TS200KS | FDA UDI | Class II | Active |
| TheraSeed®, SourceLink™ | 200LKP | FDA UDI | Class II | Active |
| QuickLink™, SourceLink™ | 70303QC20 | FDA UDI | Class II | Active |
| QuickLink™, BrachySource™ | 1251QCL | FDA UDI | Class II | Active |
| TheraSeed®, SourceLink™ | 200PAP | FDA UDI | Class II | Active |
| BrachySource™, SourceLink™ | 1251LINK | FDA UDI | Class II | Active |
| BrachySource™, SourceLink™ | 1251PAP | FDA UDI | Class II | Active |
| BrachyStar™ | 917201 | FDA UDI | Class I | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 10, 2018 | Z-1702-2018 | — | terminated | Bard Medical Division is recalling the BARD BrachySource Iodine125 Radioactive Seeds in Mick Applicators and BARD BrachySource Iodine125 Radioactive Seeds Loose in Vial with Sterile Spacers. Because the incorrect dosage level radioactive seeds were mixed up and sent to two hospitals. One Hospital ordered BrachySource Iodine125 0.36 mCi radioactive seeds but instead received BrachySource Iodine125 0.28 mCi radioactive seeds and vice versa for the other hospital affected. |