# BrachySource™ PS1251C

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/brachysource-ps1251c>
- Manufacturer: [Bard Brachytherapy, Inc](https://devicerts.com/manufacturers/fda-fei-3002942387) (FDA registration: United States)
- Device class: Class II (US FDA)
- FDA product code: KXK
- GMDN: General-purpose brachytherapy system applicator, manual (38435)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00801741078217 · listed 2015-10-05 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K093663 · decision 2009-12-23 · decision SESE · status: Active · from GUDID

## Recalls

- Z-1702-2018 · Class II · terminated · initiated 2018-04-10: 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.

## Identity

- Trade name: BrachySource™ [FDA GUDID (AccessGUDID)]
- Generic name: General-purpose brachytherapy system applicator, manual [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: PS1251C [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00801741078217 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K093663 [FDA GUDID (AccessGUDID)]
- FDA product code: KXK [FDA GUDID (AccessGUDID)]
- GMDN term: General-purpose brachytherapy system applicator, manual (38435) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 892.5730 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- Sterilisation method: Moist Heat or Steam Sterilization [FDA GUDID (AccessGUDID)]
- MRI safety: MR Conditional [FDA GUDID (AccessGUDID)]

## Properties

- Sterilise before use: Yes [FDA GUDID (AccessGUDID)]
- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Convenience kit: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: BrachySource™ PS1251C, Bard Brachytherapy, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/brachysource-ps1251c (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/brachysource-ps1251c.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/brachysource-ps1251c
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.