# Any-Com

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

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

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI B-08809518345236 · registered 2026-03-05 · status: Active
- **EUDAMED** · CE/MDD · European Union · Basic UDI-DI B-08809518345236 · registered 2026-03-05 · status: Active

## Recalls

No recall on record.

## Identity

- Device name: Dental composite resin [EUDAMED]
- Model / reference: 301 Any-Com Universal Kit [EUDAMED]; 302 Any-Com Kit [EUDAMED]; 301-1 \~ 301-21 Any-Com Refill [EUDAMED]; GB2206RC001 [EUDAMED]; 301-1 [EUDAMED]; 301-2 [EUDAMED]; 301-3 [EUDAMED]; 301-4 [EUDAMED]; 301-5 [EUDAMED]; 301-6 [EUDAMED]; 301-7 [EUDAMED]; 301-8 [EUDAMED]; 301-9 [EUDAMED]; 301-10 [EUDAMED]; 301-11 [EUDAMED]; 301-12 [EUDAMED]; 301-13 [EUDAMED]; 301-14 [EUDAMED]; 301-15 [EUDAMED]; 301-16 [EUDAMED]; 301-17 [EUDAMED]; 301-18 [EUDAMED]; 301-19 [EUDAMED]; 301-20 Any-Com Refill A1 [EUDAMED]; A2 [EUDAMED]; A3 [EUDAMED]; A3.5 [EUDAMED]; A4 [EUDAMED]; B1 [EUDAMED]; B2 [EUDAMED]; B3 [EUDAMED]; C2 [EUDAMED]; C3 [EUDAMED]; D2 [EUDAMED]; D3 [EUDAMED]; WT [EUDAMED]; OP [EUDAMED]; OA2 [EUDAMED]; OA3 [EUDAMED]; TL [EUDAMED]; A2E [EUDAMED]; A3E [EUDAMED]; B2E [EUDAMED]; 301H Any-Com Universal Kit [EUDAMED]; 302H Any-Com Kit [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 08809518345236 [EUDAMED]; 08809518340729 [EUDAMED]; 08809518340767 [EUDAMED]; 08809518340736 [EUDAMED]; 08809518340781 [EUDAMED]; 08809518340835 [EUDAMED]; 08809518340699 [EUDAMED]; 08809518340842 [EUDAMED]; 08809518340859 [EUDAMED]; 08809518340910 [EUDAMED]; 08809518340705 [EUDAMED]; 08809518340866 [EUDAMED]; 08809518340798 [EUDAMED]; 08809518340750 [EUDAMED]; 08809518340743 [EUDAMED]; 08809518344840 [EUDAMED]; 08809518344772 [EUDAMED]; 08809518340774 [EUDAMED]; 08809518340873 [EUDAMED]; 08809518340712 [EUDAMED]; 08809518340682 [EUDAMED]; 08809518340804 [EUDAMED]; 08809518340828 [EUDAMED]; 08809518340811 [EUDAMED]
- Basic UDI-DI: B-08809518345236 [EUDAMED]; 880951834RS05NM [EUDAMED]; 880951834RS10NE [EUDAMED]; 880951834RS11NG [EUDAMED]; 880951834RS19NY [EUDAMED]; 880951834RS20NH [EUDAMED]
- Direct marketing DI: 08809518340729 [EUDAMED]; 08809518340767 [EUDAMED]; 08809518340736 [EUDAMED]; 08809518345236 [EUDAMED]; 08809518340781 [EUDAMED]; 08809518340835 [EUDAMED]; 08809518340699 [EUDAMED]; 08809518340842 [EUDAMED]; 08809518340859 [EUDAMED]; 08809518340910 [EUDAMED]; 08809518340705 [EUDAMED]; 08809518340866 [EUDAMED]; 08809518340750 [EUDAMED]; 08809518340743 [EUDAMED]; 08809518344840 [EUDAMED]; 08809518344772 [EUDAMED]; 08809518340774 [EUDAMED]; 08809518340873 [EUDAMED]; 08809518340712 [EUDAMED]; 08809518340682 [EUDAMED]; 08809518340804 [EUDAMED]; 08809518340828 [EUDAMED]; 08809518340811 [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]; Italy [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, MEDICLUS Co., Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/any-com-gb2206rc001 (data as of 2026-11-14).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-11-12
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/any-com-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-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.