# Aed 8800B-Hd

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

- Canonical page: <https://devicerts.com/devices/aed-8800b-hd>
- Manufacturer: [National Advanced Endoscopy Devices, Inc.](https://devicerts.com/manufacturers/fda-fei-3000204191) (FDA registration: United States)
- Name in the registry: AED 8800B-HD
- Device class: Class II (US FDA)
- FDA product code: EOB
- GMDN: Rigid optical sinoscope (37180)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00848657076890 · listed 2026-01-15 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K170285 · decision 2017-08-01 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: AED [FDA GUDID (AccessGUDID)]
- Generic name: Rigid optical sinoscope [FDA GUDID (AccessGUDID)]
- Model / reference: 8800B-HD [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00848657076890 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K170285 [FDA GUDID (AccessGUDID)]
- FDA product code: EOB [FDA GUDID (AccessGUDID)]
- GMDN term: Rigid optical sinoscope (37180) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 874.4760 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

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

## Properties

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

## Source and citation

- Cite as: Aed 8800B-Hd, National Advanced Endoscopy Devices, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/aed-8800b-hd (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/aed-8800b-hd.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/aed-8800b-hd
- 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.