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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

12528 — Class IIa MDR by G. Pohl-Boskamp GmbH &…

MD Atlas
G. Pohl-Boskamp GmbH & Co. KG

EUDAMED last updated this device on May 12, 2026

12528

40291250012G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: G. Pohl-Boskamp GmbH & Co. KG
UDI-DI code: 04029125105403
Reference / catalog number: 12528

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View device family (Basic UDI)

Manufacturer information

Organization name: G. Pohl-Boskamp GmbH & Co. KG
SRN: DE-MF-000010001
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Denmark; available across 3 countries total.

Country	On market since	Until
DenmarkPrimary placement		Still on market
Norway		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04029125105403
Basic UDI-DI: 40291250012G
Reference / catalog number: 12528
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 1 pack contains 1 tube with 20 lozenges
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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Certificates

Certificate health across this manufacturer's portfolio.

3253GB448260430Supplemented
Quality management systemNotified body: 0482Expiry: Dec 6, 2026