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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

377738 — IVDD — General IVDD by NUNC A/S

MD Atlas
NUNC A/S

EUDAMED last updated this device on May 21, 2026

377738

B-15713311000257

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: NUNC A/S
UDI-DI code: 15713311000257
Reference / catalog number: 377738

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Manufacturer information

Organization name: NUNC A/S
SRN: DK-MF-000024621
Manufacturer status: Active

Related devices

366656B-15713311000240On the market 377224B-15713311000196On the market 368632B-15713311000219On the market 377267B-15713311000202On the market 363401B-15713311000233On 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

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

CW010
EUDAMED did not publish a description for this code.
CW999
Do not use CryoTubes in the liquid nitrogen unless correctly sealed in Nunc Cryoflex TM Tubing (cat.no. 343958). Improper use may cause enreapment of liquefied nitrogen inside the vial and lead to pressure build-up, resulting in possible explosion or biohazard release. Use appropriate safety procedures as outlined in the Nalge Nunc International Cryopreservation Manual when handling and disposing of CryoTubes.

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 15713311000257
Basic UDI-DI: B-15713311000257
Reference / catalog number: 377738
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic 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)

W050299DEVICES FOR SAMPLES TRANSPORT - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Expiration date
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Software identification