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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

2120 — Class I MDR by Dr. Jacoby GmbH & Co. KG

MD Atlas
Dr. Jacoby GmbH & Co. KG

EUDAMED last updated this device on Jul 29, 2024

2120

4033082Einreibung98

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Jacoby GmbH & Co. KG
UDI-DI code: 04033082021201
Reference / catalog number: 2120

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Manufacturer information

Organization name: Dr. Jacoby GmbH & Co. KG
SRN: DE-MF-000022659
Manufacturer status: Active

Critical warnings

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

CW011
Avoid contact with eyes, open wounds and mucous membranes. Not intended for children.

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: 04033082021201
Basic UDI-DI: 4033082Einreibung98
Reference / catalog number: 2120
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: 350 MU03

EMDN nomenclature code(s)

V0999FLUIDS/GASES FOR CLINICAL/THERAPEUTICAL USE - 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

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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.