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Organization name
UDI-DI code
Reference / catalog number

BK200KlinopurES-V — Class IIb MDR by Natur Vital Handels GmbH

MD Atlas
Natur Vital Handels GmbH

EUDAMED last updated this device on Feb 4, 2025

BK200KlinopurES-V

912012721BKMU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Natur Vital Handels GmbH
UDI-DI code: 09120127214348
Reference / catalog number: BK200KlinopurES-V

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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
Spain		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09120127214348
Basic UDI-DI: 912012721BKMU
Reference / catalog number: BK200KlinopurES-V
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.