# Any-Com Flow

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

- Canonical page: <https://devicerts.com/devices/any-com-flow-gb2206rc001>
- Manufacturer: [MEDICLUS Co., Ltd.](https://devicerts.com/manufacturers/mediclus-co-ltd) (South Korea)
- Device class: Class IIa (EU MDR / EU MDD)
- FDA product code: EBF
- EMDN: Q01010103 DENTAL RESTORATIVE COMPOSITES

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI B-08809518344178 · registered 2026-03-09 · status: Active
- **EUDAMED** · CE/MDD · European Union · Basic UDI-DI B-08809518344178 · registered 2026-03-09 · status: Active
- **510(k)** · FDA 510(k) · United States · K250823 · decision 2025-04-14 · decision SESE · status: Active
- **510(k)** · FDA 510(k) · United States · K241147 · issued 2024-09-26 · status: Active

## Recalls

No recall on record.

## Identity

- Device name: Dental composite resin [EUDAMED]
- Model / reference: 306 Any-Com Flow Kit [EUDAMED]; 306-1 \~ 306-17 Any-Com Flow Refill [EUDAMED]; 306-22 \~ 306-26 Any-Com Flow Rainbow [EUDAMED]; 309 Any-Com Flow Rainbow Kit [EUDAMED]; GB2206RC001 [EUDAMED]; 306H Any-Com Flow Kit [EUDAMED]; 306-1\~306-17 Any-Com Flow Refill (A1 [EUDAMED]; A2 [EUDAMED]; A3 [EUDAMED]; A3.5 [EUDAMED]; A4 [EUDAMED]; B1 [EUDAMED]; B2 [EUDAMED]; B3 [EUDAMED]; C2 [EUDAMED]; C3 [EUDAMED]; D2 [EUDAMED]; TL [EUDAMED]; YTL [EUDAMED]; RTL [EUDAMED]; OWT [EUDAMED]; OA2 [EUDAMED]; OA3) [EUDAMED]; 306-21\~306-26 Any-Com Flow Rainbow (Blue [EUDAMED]; Pink [EUDAMED]; Purple [EUDAMED]; Yellow [EUDAMED]; Green [EUDAMED]; Orange) [EUDAMED]; 306-8A Any-Com Flow Kit [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 08809518344178 [EUDAMED]; 08809518341085 [EUDAMED]; 08809518340934 [EUDAMED]; 08809518340958 [EUDAMED]; 08809518341115 [EUDAMED]; 08809518341122 [EUDAMED]; 08809518341078 [EUDAMED]; 08809518340941 [EUDAMED]; 08809518340972 [EUDAMED]; 08809518343850 [EUDAMED]; 08809518341023 [EUDAMED]; 08809518340996 [EUDAMED]; 08809518341030 [EUDAMED]; 08809518341016 [EUDAMED]; 08809518341009 [EUDAMED]; 08809518340989 [EUDAMED]; 08809518344680 [EUDAMED]; 08809518341054 [EUDAMED]; 08809518341061 [EUDAMED]; 08809518342228 [EUDAMED]; 08809518342921 [EUDAMED]; 08809518344437 [EUDAMED]; 08809518340965 [EUDAMED]; 08809518344352 [EUDAMED]; 08809518341108 [EUDAMED]; 08809518341047 [EUDAMED]; 08809518341092 [EUDAMED]
- Basic UDI-DI: B-08809518344178 [EUDAMED]; 880951834RS17NU [EUDAMED]; 880951834RS12NJ [EUDAMED]; 880951834RS18NW [EUDAMED]; 880951834RS13NL [EUDAMED]; 880951834RS03NH [EUDAMED]
- Direct marketing DI: 08809518344178 [EUDAMED]; 08809518341085 [EUDAMED]; 08809518340934 [EUDAMED]; 08809518340958 [EUDAMED]; 08809518341115 [EUDAMED]; 08809518341122 [EUDAMED]; 08809518341078 [EUDAMED]; 08809518340941 [EUDAMED]; 08809518340972 [EUDAMED]; 08809518343850 [EUDAMED]; 08809518341023 [EUDAMED]; 08809518340996 [EUDAMED]; 08809518341030 [EUDAMED]; 08809518341016 [EUDAMED]; 08809518341009 [EUDAMED]; 08809518340989 [EUDAMED]; 08809518344680 [EUDAMED]; 08809518341054 [EUDAMED]; 08809518341061 [EUDAMED]; 08809518342228 [EUDAMED]; 08809518342921 [EUDAMED]; 08809518344437 [EUDAMED]; 08809518340965 [EUDAMED]; 08809518344352 [EUDAMED]; 08809518341108 [EUDAMED]; 08809518341047 [EUDAMED]; 08809518341092 [EUDAMED]
- EMDN code: Q01010103 [EUDAMED]

## Classification

- Device class: Class IIa [EUDAMED]
- System or procedure pack: Procedure pack which is a device in itself [EUDAMED]
- EU registration type: Legacy device (under a directive) [EUDAMED]; Standard device [EUDAMED]
- EU market of registration: Germany [EUDAMED]

## Properties

- Implantable: No [EUDAMED]; Yes [EUDAMED]
- Supplied sterile: No [EUDAMED]
- Sterilise before use: No [EUDAMED]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]

## Source and citation

- Cite as: Any-Com Flow, MEDICLUS Co., Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/any-com-flow-gb2206rc001 (data as of 2026-11-14).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- Registry records last synced: 2026-10-25
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/any-com-flow-gb2206rc001.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/any-com-flow-gb2206rc001
- 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.