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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

1101063221 — Class I MDR by Didactic

MD Atlas
Didactic

EUDAMED last updated this device on May 12, 2026

1101063221

3661809VINGT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Didactic
UDI-DI code: 03661809019203
Reference / catalog number: 1101063221

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View device family (Basic UDI)

Manufacturer information

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

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Certificates

Certificate health across this manufacturer's portfolio.

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

Critical warnings

No critical warnings reported for this device.

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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: 03661809019203
Basic UDI-DI: 3661809VINGT
Reference / catalog number: 1101063221
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: These gloves can be used in most situations where an examination glove is required
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.

T01020201VINYL 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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