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Organization name
UDI-DI code
Reference / catalog number

10256065 — Class I MDR by Albert Hohlkörper GmbH…

MD Atlas
Albert Hohlkörper GmbH & Co. KG

EUDAMED last updated this device on Apr 22, 2026

10256065

40375664000MF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Albert Hohlkörper GmbH & Co. KG
UDI-DI code: 04037566001833
Reference / catalog number: 10256065

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Manufacturer information

Organization name: Albert Hohlkörper GmbH & Co. KG
SRN: DE-MF-000005482
Manufacturer status: Active

Related devices

8201.2.1600040375663000M8On the market 0403756600088140375663000M8On the market PIC 20 01340375662000LZOn the market PIC 20 00740375662000LZOn the market PIC 20 01140375662000LZOn 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: 04037566001833
Basic UDI-DI: 40375664000MF
Reference / catalog number: 10256065
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)

Q030199NASOPHARYNGEAL DEVICES - 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.