# C-Section Recovery Kit > Active: European Union. Medical device record on deviCERTS, compiled from public registries. - Canonical page: - Manufacturer: [Fridababy, LLC](https://devicerts.com/manufacturers/fridababy-llc) (United States) - Device class: Class IIa (EU MDR) - EMDN: V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER ## Registrations and authorizations - **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 122000022PROJ117MM · UDI-DI 01220000220461 · registered 2026-06-15 · status: Active ## Recalls No recall on record. ## Identifiers - Primary DI / UDI-DI: 01220000220461 [EUDAMED] - Basic UDI-DI: 122000022PROJ117MM [EUDAMED] - EMDN code: V9099 [EUDAMED] ## Classification - Device class: Class IIa [EUDAMED] - System or procedure pack: Procedure pack [EUDAMED] - EU registration type: System or procedure pack [EUDAMED] - Medical purpose: C-Section Recovery Kit [EUDAMED] ## Properties - Supplied sterile: No [EUDAMED] - Sterilise before use: No [EUDAMED] ## Source and citation - Cite as: C-Section Recovery Kit, Fridababy, LLC. deviCERTS medical device catalogue. https://devicerts.com/devices/c-section-recovery-kit-00220461 (data as of 2026-11-14). - Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed) - Registry records last synced: 2026-10-22 - Statuses computed as of: 2026-11-14 - 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/c-section-recovery-kit-00220461 - 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.