# Perfusion Adapter Set 301022NS

> Listed: FDA GUDID listing, no authorization on record. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/perfusion-adapter-set-331022ns>
- Manufacturer: [Novosci Corp.](https://devicerts.com/manufacturers/novosci-corp) (United States, FDA applicant)
- Name in the registry: PERFUSION ADAPTER SET 301022NS
- Device class: Class II (US FDA)
- FDA product code: DWF
- GMDN: Cardioplegia solution administration adaptor (58824)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI B066301022NS1 · listed 2015-10-09 · status: Listed (GUDID: in commercial distribution)

## Recalls

No recall on record.

## Identity

- Trade name: PERFUSION ADAPTER SET [FDA GUDID (AccessGUDID)]
- Generic name: Cardioplegia solution administration adaptor [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 301022NS [FDA GUDID (AccessGUDID)]; 331022NS [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: B066301022NS1 [FDA GUDID (AccessGUDID)]
- FDA product code: DWF [FDA GUDID (AccessGUDID)]
- GMDN term: Cardioplegia solution administration adaptor (58824) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 870.4210 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- Sterilisation method: Ethylene Oxide [FDA GUDID (AccessGUDID)]

## Properties

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

## Source and citation

- Cite as: Perfusion Adapter Set 301022NS, Novosci Corp. deviCERTS medical device catalogue. https://devicerts.com/devices/perfusion-adapter-set-331022ns (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/perfusion-adapter-set-331022ns.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/perfusion-adapter-set-331022ns
- 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.