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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

25057K — Class IIa MDD by Schaefers Medizintechnik…

MD Atlas
Schaefers Medizintechnik GmbH

EUDAMED last updated this device on Jan 28, 2023

25057K

B-111751033737

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Schaefers Medizintechnik GmbH
UDI-DI code: 111751033737
Reference / catalog number: 25057K

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Manufacturer information

Organization name: Schaefers Medizintechnik GmbH
SRN: DE-MF-000006991
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 111751033737
Basic UDI-DI: B-111751033737
Reference / catalog number: 25057K
Issuing entity: IFA

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: http://www.schaefers-medizintechnik.de/downloads/TD_Schlauchsystem_T2-02-05_Gebrauchsanweisung_tubesystem_25057K_2022-03-09_Rev_NL_SJ.pdf
Additional information URL: http://www.schaefers-medizintechnik.de/downloads/TD_Schlauchsystem_T2-02-05_Gebrauchsanweisung_tubesystem_25057K_2022-03-09_Rev_NL_SJ.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A0380TUBULAR DEVICES - ACCESSORIES

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

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Expiration date
Manufacturing date
Serial number
Software identification