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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

FW26301 — Class I MDR by C. H. Müller Industries…

MD Atlas
C. H. Müller Industries GmbH

EUDAMED last updated this device on Jan 16, 2026

FW26301

426238301STERILFOLIE_01SC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C. H. Müller Industries GmbH
UDI-DI code: 04262383010328
Reference / catalog number: FW26301

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Manufacturer information

Organization name: C. H. Müller Industries GmbH
SRN: DE-MF-000027887
Manufacturer status: Active

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW030
Intended users must be healthcare professionals. The product is not intended for use by patients or lay persons.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04262383010328
Basic UDI-DI: 426238301STERILFOLIE_01SC
Reference / catalog number: FW26301
Issuing entity: GS1

Classification

Risk category: Class I
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)

T030199COVERS, INSTRUMENTS AND EQUIPMENT - 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

Related devices

FW26280426238301STERILFOLIE_01SCOn the market FW26281426238301STERILFOLIE_01SCOn the market FW26287426238301STERILFOLIE_01SCOn the market FW26288426238301STERILFOLIE_01SCOn the market FW26374426238301STERILFOLIE_01SCOn the market

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.