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Spatule de Nagahara

EUDAMEDFDA UDI

Class I (EU MDR)

Ref M32390Model 18070

by Moria S.A.

Identity

Trade Name
Spatule de Nagahara EUDAMED
MORIA FDA UDI
Generic Name
General-purpose surgical spatula FDA UDI
Device Name
WARING IRIS SPATULA EUDAMED
Model / Reference
18070 EUDAMED
M32390 EUDAMED
Nagahara Spatula FDA UDI

Identifiers

Catalog Number
M32390 FDA UDI
Primary DI / UDI-DI
03700483610877 EUDAMEDFDA UDI
Basic UDI-DI
37004836Spatulas1NJ EUDAMED
Direct Marketing DI
03700483610877 EUDAMED
FDA Product Code
HNQ FDA UDI
EMDN Code
L1706 OPHTHALMOLOGY SPATULAS, 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

Spatule de Nagahara 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

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Manufacturer

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

Sources (2)

  • EUDAMED cd749b05-f231-49c3-b5a1-00d97d3b0bc6 61 fields · synced Jul 29, 2026
  • FDA UDI 8e23f1fd-1d91-46cd-8621-4ce2085fd000 33 fields · synced May 30, 2026