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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

85139924 — Class IIa MDR by Ascensia Diabetes Care…

MD Atlas
Ascensia Diabetes Care Holdings AG

EUDAMED last updated this device on Apr 30, 2026

85139924

15016003LADEVDS28

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ascensia Diabetes Care Holdings AG
UDI-DI code: 05016003670107
Reference / catalog number: 85139924

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Manufacturer information

Organization name: Ascensia Diabetes Care Holdings AG
SRN: CH-MF-000034124
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.
CW008
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Sweden; available across 3 countries total.

Country	On market since	Until
SwedenPrimary placement		Still on market
Finland		Still on market
Norway		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05016003670107
Basic UDI-DI: 15016003LADEVDS28
Reference / catalog number: 85139924
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: Blodprovstagare
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

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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.