We have developed the 16F12 mouse monoclonal antibody (mAb), which targets the Müllerian-inhibiting substance receptor, type II (MISRII), expressed by ovarian tumors. Here, we assessed in preclinical models the possibility of using radiolabeled 16F12 in a theranostic approach for small-volume ovarian peritoneal carcinomatosis, such as after cytoreductive surgery. DOTA-, DTPA- or deferoxamine mesylate-conjugated 16F12 mAb was radiolabeled with β-particle (Lu) or α-particle (Bi) emitters for therapeutic use and with Zr for PET imaging. On the 13th postxenograft day, mice bearing intraperitoneal MISRII-positive AN3CA endometrial carcinoma cell xenografts were treated by conventional intraperitoneal radioimmunotherapy (IP-RIT) with 10 MBq ofLu-16F12 or 12.9 MBq of Bi-16F12 or by brief intraperitoneal radioimmunotherapy (BIP-RIT) using 50 MBq ofLu-16F12 or 37 MBq of Bi-16F12. For BIP-RIT, 30 min after injection of the radiolabeled mAbs, the peritoneal cavity was washed to remove the unbound radioactivity. The biodistribution ofLu- and Bi-16F12 mAbs was determined and then used for dose assessment. Hematologic toxicity was also monitored. The 16F12 mAb was satisfactorily radiolabeled for both therapy and imaging. IP-RIT with Lu-16F12 was slightly more efficient in delaying tumor growth than IP-RIT withBi-16F12. Conversely, Bi-16F12 was more efficient thanLu-16F12 in BIP-RIT. The biodistribution analysis showed that the tumor-to-blood uptake ratio was significantly higher with BIP-RIT than with IP-RIT for both Bi- andLu-16F12. Hematologic toxicity was more pronounced with Lu-16F12 than withBi-16F12. SPECT/CT images (after BIP-RIT with Lu-16F12) and PET/CT images (after injection ofZr-16F12 in the tail vein) showed focal uptake at the tumor site. Radiolabeled 16F12 could represent a new theranostic tool for small-volume ovarian peritoneal carcinomatosis. Specifically,Bi-16F12-based BIP-RIT could be proposed to selected patients as an alternative adjuvant treatment immediately after cytoreductive surgery. An anti-MISRII mAb is currently being used in a first-in-human study, thus making radiolabeled anti-MISRII mAbs a realistic theranostic option for the clinic.