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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

11507-AR240001 — Class I MDR by Remy & Geiser GmbH

MD Atlas
Remy & Geiser GmbH

EUDAMED last updated this device on May 18, 2026

11507-AR240001

426255637PIPETTETA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Remy & Geiser GmbH
UDI-DI code: 04262556372802
Reference / catalog number: 11507-AR240001

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Manufacturer information

Organization name: Remy & Geiser GmbH
SRN: DE-MF-000020726
Manufacturer status: Active

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8498M-AR240001426255637BRUSHCWOn the market 3754M-AR240001426255637BRUSHCWOn the market 4446M-AR240001426255637BRUSHCWOn the market 9389M-AR240001426255637BRUSHCWOn the market 10246M-AR240001426255637BRUSHCWOn the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262556372802
Basic UDI-DI: 426255637PIPETTETA
Reference / catalog number: 11507-AR240001
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: 50
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)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

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.