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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

2210 — Class IIa MDD by VOCO GmbH

MD Atlas
VOCO GmbH

EUDAMED last updated this device on Apr 21, 2026

2210

B-E22122101

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VOCO GmbH
UDI-DI code: E22122101
Reference / catalog number: 2210

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Manufacturer information

Organization name: VOCO GmbH
SRN: DE-MF-000008601
Manufacturer status: Active

Related devices

2451B-E22124511On the market 2424B-E22124241On the market 2453B-E22124531On the market 2454B-E22124541On the market 2423B-E22124231On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: E22122101
Basic UDI-DI: B-E22122101
Reference / catalog number: 2210
Issuing entity: HIBCC

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: set: powder 60g, liquid bottle 40 mL, conditioner bottle 20 mL
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: set: powder bottle, weight: 60g, liquid bottle Volume: 40 mL, conditioner bottle Volume: 20 mL

EMDN nomenclature code(s)

Q010280PROSTHETIC DENTISTRY DEVICES - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification