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Pince Action Croisee 9.0 Mm Corydon
EUDAMEDFDA UDIClass I (EU MDR)
Ref 20050/9.0Model 2183
by Moria S.A.
Identity
- Trade Name
- PINCE ACTION CROISEE 9.0 MM CORYDON EUDAMEDMORIA FDA UDI
- Generic Name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Forcep. curved. serrated jaws 1 mm EUDAMED
- Model / Reference
- 2183 EUDAMED20050/9.0 EUDAMEDCROSS ACTION FORCEPS 9.0 MM CORYDON FDA UDI
Identifiers
- Catalog Number
- 20050/9.0 FDA UDI
- Primary DI / UDI-DI
- 03700483628339 EUDAMEDFDA UDI
- Basic UDI-DI
- 37004836Forceps1C2 EUDAMED
- Direct Marketing DI
- 03700483628339 EUDAMED
- FDA Product Code
- HNR FDA UDI
- EMDN Code
- L170299 OPHTHALMOLOGY FORCEPS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Pince Action Croisee 9.0 Mm Corydon by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 37004836Forceps1C2 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Moria S.A.
- EUDAMED SRN
- FR-MF-000000336
Sources (2)
- EUDAMED 59f9f20c-bdb2-426e-a220-8902a0de2586 61 fields · synced Jul 22, 2026
- FDA UDI f23c2256-91f3-4af6-9151-87c35a48490a 33 fields · synced May 30, 2026