# IDG/Sanzay 1

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

- Canonical page: <https://devicerts.com/devices/idg-sanzay-c413>
- Manufacturer: [IDG/SANZAY Corporation](https://devicerts.com/manufacturers/idg-sanzay-corporation) (FDA registration: United States)
- Device class: Class I (US FDA)
- FDA product code: KNK
- GMDN: Uric acid IVD, reagent (53586)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00850053916168 · listed 2024-01-12 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K914158 · decision 1992-02-21 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: IDG/Sanzay [FDA GUDID (AccessGUDID)]
- Generic name: Uric acid IVD, reagent [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 1 [FDA GUDID (AccessGUDID)]; C413 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00850053916168 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K914158 [FDA GUDID (AccessGUDID)]
- FDA product code: KNK [FDA GUDID (AccessGUDID)]
- GMDN term: Uric acid IVD, reagent (53586) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class I [FDA GUDID (AccessGUDID)]
- Regulation number: 862.1775 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Dimensions & Sizes

- Size: Total Volume — 100 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 120 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 240 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 250 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 480 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 500 Milliliter [FDA GUDID (AccessGUDID)]; Total Volume — 1 Liter [FDA GUDID (AccessGUDID)]

## Properties

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

## Source and citation

- Cite as: IDG/Sanzay 1, IDG/SANZAY Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/idg-sanzay-c413 (data as of 2026-11-15).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/idg-sanzay-c413.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/idg-sanzay-c413
- 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.