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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

Adjustable plast. speculum — Class I MDR by Moria S.A.

MD Atlas
Moria S.A.

EUDAMED last updated this device on Oct 31, 2025

Adjustable plast. speculum

37004836Speculums2WZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Moria S.A.
UDI-DI code: 03700483601431
Reference / catalog number: 17231X10

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Manufacturer information

Organization name: Moria S.A.
SRN: FR-MF-000000336
Manufacturer status: Active

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Adjustable plast. speculum
UDI-DI code: 03700483601431
Basic UDI-DI: 37004836Speculums2WZ
Reference / catalog number: 17231X10
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: Single use instrument for ophthalmic surgery
Additional information URL: https://www.moria-surgical.com/resources-center?types[0]=3&page=1&limit=12&_=1761730662608
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.

Q0299OPHTHALMIC 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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