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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

21941 — Class I MDD by Primed Halberstadt…

MD Atlas
Primed Halberstadt Medizintechnik GmbH

EUDAMED last updated this device on Apr 30, 2026

21941

B-04250203201582

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Primed Halberstadt Medizintechnik GmbH
UDI-DI code: 04250203201582
Reference / catalog number: 21941

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Manufacturer information

Organization name: Primed Halberstadt Medizintechnik GmbH
SRN: DE-MF-000004967
Manufacturer status: Active

Related devices

15909B-04250203260831On the market 15941B-04250203261166On the market 15933B-04250203260954On the market 15931B-04250203261043On the market 15938B-04250203261104On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250203201582
Basic UDI-DI: B-04250203201582
Reference / catalog number: 21941
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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)

A060301COLLECTION BAGS AND OTHER CONTAINERS FOR DRAINAGES AND FISTULAS, SINGLE USE

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.