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Canule Binkhorst-Quintana. coudée à droite. Diam. 0.5mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 13250Model 791

by Moria S.A.

Identity

Trade Name
Canule Binkhorst-Quintana. coudée à droite. Diam. 0.5mm EUDAMED
MORIA FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
Galezowski Cannula curved EUDAMED
Model / Reference
791 EUDAMED
13250 EUDAMED
Binkhorst-Quintana Cannula, curved on the right, irrigation at 11 o'clock, diame FDA UDI

Identifiers

Catalog Number
13250 FDA UDI
Primary DI / UDI-DI
03700483604982 EUDAMEDFDA UDI
Basic UDI-DI
37004836Cannulas16L EUDAMED
FDA Product Code
HMX FDA UDI
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE EUDAMED
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Canule Binkhorst-Quintana. coudée à droite. Diam. 0.5mm by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moria S.A.
EUDAMED SRN
FR-MF-000000336

Sources (2)

  • EUDAMED d14aa18d-8da5-4ba8-a8c3-b8c104637a4c 61 fields · synced Jul 9, 2026
  • FDA UDI 465a7630-c4b1-4bf6-b579-4880066123b3 33 fields · synced May 30, 2026