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Organization name
UDI-DI code
Reference / catalog number

BK600SE — Class IIb MDR by Natur Vital Handels GmbH

MD Atlas
Natur Vital Handels GmbH

EUDAMED last updated this device on Feb 7, 2025

BK600SE

912012721BKMU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Natur Vital Handels GmbH
UDI-DI code: 09120127218346
Reference / catalog number: BK600SE

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Manufacturer information

Organization name: Natur Vital Handels GmbH
SRN: AT-MF-000026484
Manufacturer status: Active

Related devices

BK200NO912012721BKMUOn the market BK600NO912012721BKMUOn the market BK600PRT912012721BKMUOn the market BK200PRT912012721BKMUOn the market BK600RO912012721BKMUOn the market

Critical warnings

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

CW159
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.
CW148
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09120127218346
Basic UDI-DI: 912012721BKMU
Reference / catalog number: BK600SE
Issuing entity: GS1

Classification

Risk category: Class IIb
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)

G0402ORALLY ADMINISTERED DEVICES FOR APPETITE CONTROL AND REDUCTION OF INTESTINAL ABSORPTION

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.