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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

Jayle Forceps. with facing teeth… — Class I MDR by Moria S.A.

MD Atlas
Moria S.A.

EUDAMED last updated this device on Dec 2, 2025

Jayle Forceps. with facing teeth 0.8 mm and tying platforms

37004836Forceps1C2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Moria S.A.
UDI-DI code: 03700483604289
Reference / catalog number: 3222

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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.

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: Jayle Forceps. with facing teeth 0.8 mm and tying platforms
UDI-DI code: 03700483604289
Basic UDI-DI: 37004836Forceps1C2
Reference / catalog number: 3222
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: Reusable 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.

EMDN nomenclature code(s)

L170299OPHTHALMOLOGY FORCEPS, REUSABLE - 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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