← Back to catalogue

Intraoral Rhodium Plated Superelastic Archwire Large - NiTi Rec. 0.48 X 0.63mm …

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 50.62.137Model THREADS AND BOWS - Class I

by Dental Morelli Ltda.

Identity

Trade Name
Intraoral Rhodium Plated Superelastic Archwire Large - NiTi Rec. 0.48 X 0.63mm (.019 X .025") EUDAMED
Morelli FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
Intraoral Rhodium Plated Superelastic Archwire Large - NiTi Rec. 0.48 X 0.63mm (.019 X .025") FDA UDI
Model / Reference
THREADS AND BOWS - Class I EUDAMED
50.62.137 EUDAMEDFDA UDI
Description
Intraoral Rhodium Plated Superelastic Archwire Large - NiTi Rec. 0.48 X 0.63mm (.019 X .025") FDA UDI

Identifiers

Catalog Number
50.62.137 FDA UDI
Primary DI / UDI-DI
07895742252458 EUDAMEDFDA UDI
Basic UDI-DI
B-07895742252458 EUDAMED
7895742130FT EUDAMED
FDA Product Code
DZC FDA UDI
EMDN Code
Q010405 ORTHODONTIC WIRES EUDAMED
GMDN Term
Orthodontic archwire FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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

Intraoral Rhodium Plated Superelastic Archwire Large - NiTi Rec. 0.48 X 0.63mm … by Dental Morelli Ltda. — Class I — MDR, MDD, FDA UDI — listed in EUDAMED…

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

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

Sources (3)

  • EUDAMED 75f70be5-1bfd-48b1-8955-0edbd20a1f7c 61 fields · synced Jul 9, 2026
  • EUDAMED 91081e49-2d7f-42ce-9672-e5fd75f98152 61 fields · synced May 19, 2026
  • FDA UDI def176f6-a271-4b9d-badf-f24a4096d7f8 35 fields · synced May 30, 2026