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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

MGH3050/PO — Class I MDR by Didactic

MD Atlas
Didactic

EUDAMED last updated this device on May 13, 2026

MGH3050/PO

3661809PE3DV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Didactic
UDI-DI code: 03661809018619
Reference / catalog number: MGH3050/PO

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View device family (Basic UDI)

Manufacturer information

Organization name: Didactic
SRN: FR-MF-000000176
Manufacturer status: Active

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03661809018619
Basic UDI-DI: 3661809PE3DV
Reference / catalog number: MGH3050/PO
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: Polyethylene glove 500mm, male size, box of 200 units. This device is intended for healthcare examination tasks and procedures that do not require sterile conditions.
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.

T01020202POLYETHYLENE EXAMINATION / TREATMENT GLOVES

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.

ECM25MDR014Withdrawn
Quality management systemNotified body: 1282Expiry: Jul 28, 2030