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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

AcDrop — Class I MDR by Aero Pump GmbH

MD Atlas
Aero Pump GmbH

EUDAMED last updated this device on May 19, 2026

AcDrop

426242274AD001SP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aero Pump GmbH
UDI-DI code: 04262422740001
Reference / catalog number: 70023700MD

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Manufacturer information

Organization name: Aero Pump GmbH
SRN: DE-MF-000034723
Manufacturer status: Active

Related devices

AcDrop426242274AD001SPOn the market AcDrop426242274AD001SPOn the market AcDrop426242274AD001SPOn the market 60042500MD426242274AD001SPOn the market AcDrop426242274AD001SPOn 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.

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.

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: AcDrop
UDI-DI code: 04262422740001
Basic UDI-DI: 426242274AD001SP
Reference / catalog number: 70023700MD
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: 500
Additional product description: AcDrop® is used to be combined with the compatible containers (bottles) and formulations (liquids) for various application field (e.g., nasal or ophthalmological application).
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Delivered Dose — 30 MU37

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