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Kit Tubulure d'infusion pour Ch. Artif.
EUDAMEDFDA UDIClass I (EU MDR)
Ref 19181Model 19138
by Moria S.A.
Identity
- Trade Name
- Kit Tubulure d'infusion pour Ch. Artif. EUDAMEDONE FDA UDI
- Generic Name
- Corneal resection holder, single-use FDA UDI
- Device Name
- Evolution 2 - 3 - 3e Tubing EUDAMED
- Model / Reference
- 19138 EUDAMED19181 EUDAMEDINFUSION TUBING SET FOR ARTIFICIAL CHAMBER FDA UDI
Identifiers
- Catalog Number
- 19181 FDA UDI
- Primary DI / UDI-DI
- 03700483602162 EUDAMEDFDA UDI
- Basic UDI-DI
- 37004836TubingDV EUDAMED
- FDA Product Code
- HRH FDA UDI
- EMDN Code
- Q020299 CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHER EUDAMED
- GMDN Term
- Corneal resection holder, single-use 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
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Kit Tubulure d'infusion pour Ch. Artif. 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 | 37004836TubingDV | 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 e9de22b6-c6a8-434a-9796-3cb1c4f8b7e2 61 fields · synced Jul 23, 2026
- FDA UDI c61e9e9e-b74f-4479-93ee-157049f89e23 33 fields · synced May 29, 2026