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Intraora Archwire Superelastic Large NiTi - Rectangular 0, 43x0, 63mm (.017"x.0…

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 50.62.012Model WIRES AND BOWS - Class IIa

by Dental Morelli Ltda.

Identity

Trade Name
Intraora Archwire Superelastic Large NiTi - Rectangular 0,43x0,63mm (.017"x.025") EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
Intraora Archwire Superelastic Large NiTi - Rectangular 0,43x0,63mm (.017"x.025") FDA UDI
Model / Reference
WIRES AND BOWS - Class IIa EUDAMED
50.62.012 EUDAMEDFDA UDI
Description
Intraora Archwire Superelastic Large NiTi - Rectangular 0,43x0,63mm (.017"x.025") FDA UDI

Identifiers

Catalog Number
50.62.012 FDA UDI
Primary DI / UDI-DI
07895742000134 EUDAMEDFDA UDI
Basic UDI-DI
7895742172GB EUDAMED
B-07895742000134 EUDAMED
FDA Product Code
DZC FDA UDI
EMDN Code
Q010405 ORTHODONTIC WIRES EUDAMED
GMDN Term
Orthodontic archwire FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Intraora Archwire Superelastic Large NiTi - Rectangular 0, 43x0, 63mm (.017"x.0… by Dental Morelli Ltda. — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED…

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
BR-MF-000004812
Authorised Representative
Nuno Flores PT-AR-000003118

Sources (3)

  • EUDAMED 4f0825aa-a5f9-449f-982e-6b68155e909b 61 fields · synced Jul 13, 2026
  • EUDAMED 13a49e9e-958d-4b4b-a946-eea20ddb05b1 61 fields · synced May 19, 2026
  • FDA UDI a6a654ae-ae68-4430-880f-b974cf9f58e9 35 fields · synced May 30, 2026