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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

3770035346875 — Class I MDR by ID INDUSTRIE SAS

MD Atlas
ID INDUSTRIE SAS

EUDAMED last updated this device on Feb 24, 2026

3770035346875

3770016799DM278

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ID INDUSTRIE SAS
UDI-DI code: 03770035346875
Reference / catalog number: 3770035346875

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Manufacturer information

Organization name: ID INDUSTRIE SAS
SRN: FR-MF-000040421
Manufacturer status: Active

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Critical warnings

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

CW999
Tenir hors de portée des enfants. Ne pas prélever directement dans le flacon. Verser dans un récipient propre avant utilisation

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03770035346875
Basic UDI-DI: 3770016799DM278
Reference / catalog number: 3770035346875
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Flacon de 1L de serum physiologique, NaCL 0,9%, non stérile
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

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.