Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Alveolate Forceps — Class I MDR by Moria S.A.

MD Atlas
Moria S.A.

EUDAMED last updated this device on Oct 31, 2025

Alveolate Forceps

37004836Forceps2C4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Moria S.A.
UDI-DI code: 03700483612116
Reference / catalog number: 17514X5

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

10 stainless steel wire for ref. 417437004836Loops2POn the market 2 gaskets for 1716937004836Trephines4XAOn the market Abadie Curette. small model37004836CurettesLGOn the market ACP footswitchB-19189H7On the market ACP systemB-03700483629183On the market

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: Alveolate Forceps
UDI-DI code: 03700483612116
Basic UDI-DI: 37004836Forceps2C4
Reference / catalog number: 17514X5
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.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification