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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

75015DJNQ — Class IIa MDR by Lallemand Pharma

MD Atlas
Lallemand Pharma

EUDAMED last updated this device on Apr 28, 2026

75015DJNQ

76401497215RT

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lallemand Pharma
UDI-DI code: 07640149724370
Reference / catalog number: 75015DJNQ

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Manufacturer information

Organization name: Lallemand Pharma
SRN: CH-MF-000036587
Manufacturer status: Active

Critical warnings

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

CW999
Да не се използва при деца и юноши под 18-годишна възраст.
CW999
Да не се използва при свръхчувствителност или алергия към една или няколко съставки.
CW999
По време на употребата на изделието да не се използват други назални продукти/лекарства.

Market distribution

Primary placement in Bulgaria; available across 1 country total.

Country	On market since	Until
BulgariaPrimary placement	Oct 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07640149724370
Basic UDI-DI: 76401497215RT
Reference / catalog number: 75015DJNQ
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 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)

Q030103NASAL IRRIGATION SOLUTIONS

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

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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.