Moria S.A.
Active in EUDAMEDFrancefrom SRN EUDAMED FDA SRN FR-MF-000000336 FEI 3003289411
Moria S.A. is a medical device manufacturer based in France, with 764 devices listed in EUDAMED and FDA GUDID (EU Class I and IIa) as of 12 Nov 2026.
- Devices
- 764
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 764
- FDA GUDID 513
- Device classes
- EU Class I 593
- EU Class IIa 171
- Top EMDN categories
- Identifiers
- EUDAMED SRN FR-MF-000000336
- FDA FEI 3003289411
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
What Moria S.A. makes
Moria S.A. manufactures reusable and single-use ophthalmic surgical instruments, including corneal markers, punch sets, suturing needle holders, and ocular manipulation tools. Their reusable devices include non-illuminating suction cannulas, spatulas, and curettes designed for corneal and intraocular procedures. Single-use kits are non-medicated and intended for specific surgical applications. The company also produces specialized forceps, hooks, and storage solutions for intraocular lenses.
The portfolio comprises Class I and Class IIa medical devices, regulated under EU medical device directives. All listed devices are registered in the EU’s eudamed database. The company is based in France.
Catalogue
Search and filter all 764 devicesShowing 1-50 of 764
Company details
- EUDAMED SRN
- FR-MF-000000336
- FDA FEI number
- 3003289411
- EU VAT number
- FR48602035750
- EUDAMED status
- Active
- EUDAMED registered name
- Moria S.A.
- Registered address
- 27, Rue du Pied de Fourche, 03160, BOURBON L'ARCHAMBAULT, France
- pjay@moria-int.com
- PRRC contact
- Pascal JAY
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 2 May 2029
GMED SAS 0459 1 certificate
- 39713 Active
Quality management system EU MDR
- Issued
- 7 Jul 2026
- Expires
- 2 May 2029
- Reason
- Other
Frequently asked questions
How many devices does Moria S.A. have in the registry?
The registry currently lists 764 devices for Moria S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moria S.A.'s devices?
Among its 50 most recently registered devices, Moria S.A. has devices listed in EUDAMED (50 devices) and FDA GUDID (36 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Moria S.A.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Moria S.A.'s devices are Class I and Class IIa. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Moria S.A.?
EUDAMED lists 1 certificate for Moria S.A. (quality management system) under MDR. The most recent was issued on 7 Jul 2026.
What are the newest devices from Moria S.A. in the registry?
The most recently registered devices listed for Moria S.A. include GOOSEY FORCEPS, Marqueur cornée diam 8 mm, Ciseaux de Barraquer. à 2 lames mousses and Phaco cliveur de Haefliger (pour gaucher).