# A Plus 1

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

- Canonical page: <https://devicerts.com/devices/a-plus-sp-0251-6s>
- Manufacturer: [A Plus International, Inc](https://devicerts.com/manufacturers/fda-fei-2083545) (FDA registration: United States)
- Device class: Class I (US FDA)
- FDA product code: GDY
- GMDN: Dissection sponge (13698)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00683534870020 · listed 2022-10-19 · status: Listed (GUDID: in commercial distribution)

## Recalls

No recall on record.

## Identity

- Trade name: A Plus [FDA GUDID (AccessGUDID)]
- Generic name: Dissection sponge [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 1 [FDA GUDID (AccessGUDID)]; SP-0251-6S [FDA GUDID (AccessGUDID)]
- Description: A PLUS - Specialty Sponges , 9/16", Bleached White , Kittner, X-Ray Detectable, Steam Pretreatment, 100 Pc(s)/Bag, 1000 Pc(s)/Case [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00683534870020 [FDA GUDID (AccessGUDID)]
- FDA product code: GDY [FDA GUDID (AccessGUDID)]
- GMDN term: Dissection sponge (13698) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class I [FDA GUDID (AccessGUDID)]
- Regulation number: 878.4450 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Sterilise before use: Yes [FDA GUDID (AccessGUDID)]
- Single use: Yes [FDA GUDID (AccessGUDID)]
- Premarket exempt: 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)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: A Plus 1, A Plus International, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/a-plus-sp-0251-6s (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/a-plus-sp-0251-6s.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/a-plus-sp-0251-6s
- 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.