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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

1414 — Class I MDR by ALLERGIKA Pharma GmbH

MD Atlas
ALLERGIKA Pharma GmbH

EUDAMED last updated this device on Sep 24, 2024

1414

PP1354514151654

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALLERGIKA Pharma GmbH
UDI-DI code: 110192088954
Reference / catalog number: 1414

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Manufacturer information

Organization name: ALLERGIKA Pharma GmbH
SRN: DE-MF-000016908
Manufacturer status: Active

Related devices

1473PP1354514151654On the market 1498PP1354514151654On the market 1427PP1354514151654On the market 1497PP1354514151654On the market 1494PP1354514151654On the market

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: 110192088954
Basic UDI-DI: PP1354514151654
Reference / catalog number: 1414
Issuing entity: IFA

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: https://www.allergika.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0299PROTECTION DRAPES AND GARMENTS - 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

Certificate health across this manufacturer's portfolio.

44911230005Issued
Quality management systemNotified body: 0044Expiry: May 6, 2031