← Back to catalogue

Mini Dilateur de Pupille de Beehler. courbe

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 19009/2.8Model 19009

by Moria S.A.

Identity

Trade Name
Mini Dilateur de Pupille de Beehler. courbe EUDAMED
MORIA FDA UDI
Generic Name
General-purpose surgical spatula FDA UDI
Device Name
Beehler Pupil Dilator. straight EUDAMED
Model / Reference
19009 EUDAMED
19009/2.8 EUDAMED
Micro Beehler Pupil Dilator, curved FDA UDI

Identifiers

Catalog Number
19009/2.8 FDA UDI
Primary DI / UDI-DI
03700483608829 EUDAMEDFDA UDI
Basic UDI-DI
37004836Iris-Retractors5U EUDAMED
Direct Marketing DI
03700483608829 EUDAMED
FDA Product Code
HNI FDA UDI
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE EUDAMED
GMDN Term
General-purpose surgical spatula 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

Mini Dilateur de Pupille de Beehler. courbe 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 7d2f5222-a95d-4744-a289-139173c3b8f8 61 fields · synced Jul 29, 2026
  • FDA UDI 8d0fb310-b222-45bc-bca2-a42105add96a 33 fields · synced May 30, 2026