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Organization name
UDI-DI code
Reference / catalog number

0032342 — Class IIa MDD by lege artis Pharma GmbH…

MD Atlas
lege artis Pharma GmbH + Co. KG

EUDAMED last updated this device on Mar 26, 2026

0032342

B-111247264926

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: lege artis Pharma GmbH + Co. KG
UDI-DI code: 111247264926
Reference / catalog number: 0032342

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Manufacturer information

Organization name: lege artis Pharma GmbH + Co. KG
SRN: DE-MF-000006175
Manufacturer status: Active

Critical warnings

16 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW132
The safety data sheet can be downloaded from www.legeartis.de or requested by E-Mail from sicherheitsdatenblaetter@legeartis.de.
CW135
EUDAMED did not publish a description for this code.
CW318
EUDAMED did not publish a description for this code.
CW193
EUDAMED did not publish a description for this code.
CW353
Allow to drink plenty of water in small sips (dilution effect).
CW414
EUDAMED did not publish a description for this code.
CW305
EUDAMED did not publish a description for this code.
CW334
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW397
EUDAMED did not publish a description for this code.
CW999
Contra-indication: Allergies to chlorine
CW999
Contra-indication: Open apical foramen
CW999
Avoid contact of sodium hypochlorite solution with mucous membrane, skin and eyes as well as the penetration into the periapical tissue.
CW011
irritant
CW999
Do not pour back residues of the solution into the bottle.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Slovakia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 111247264926
Basic UDI-DI: B-111247264926
Reference / catalog number: 0032342
Issuing entity: IFA

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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010199CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

0032301PP01991.LA10.CLB2.ENDO.31On the market 0032312B-111669984158On the market 0032343B-111247265589On the market 0032304B-111669969204On the market 0032318B-110367214880On 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.