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Porte-aiguilles de Troutman-O'Brien. courbe. sans verrou

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9960Model 2484

by Moria S.A.

Identity

Trade Name
Porte-aiguilles de Troutman-O'Brien. courbe. sans verrou EUDAMED
MORIA FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Vantey-Desvignes Needle Holder. with wide jaws EUDAMED
Model / Reference
2484 EUDAMED
9960 EUDAMED
Troutman-O'Brien Needle Holder, curved, without lock FDA UDI

Identifiers

Catalog Number
9960 FDA UDI
Primary DI / UDI-DI
03700483604692 EUDAMEDFDA UDI
Basic UDI-DI
37004836Needle-Holders1AQ EUDAMED
Direct Marketing DI
03700483604692 EUDAMED
FDA Product Code
HNM FDA UDI
EMDN Code
L0205 NEEDLE HOLDERS, REUSABLE EUDAMED
GMDN Term
Suturing needle holder, 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: Suturing needle holder, reusable

Porte-aiguilles de Troutman-O'Brien. courbe. sans verrou by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing needle holder, 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 76d41583-b79d-4c9e-aacf-61d12fccae76 61 fields · synced Jul 22, 2026
  • FDA UDI 8e4ed91b-31b9-44da-b985-49b038fc4dde 33 fields · synced May 30, 2026