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Morelli

FDA UDI

Class I (US FDA UDI)

by Dental Morelli Ltda

Identity

Trade Name
Morelli FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
Intraoral Archwire Copper NiTi 35°C - Upper - Rectangular 0,40x0,55mm (.016"x.022") FDA UDI
Model / Reference
50.62.151 FDA UDI
Description
Intraoral Archwire Copper NiTi 35°C - Upper - Rectangular 0,40x0,55mm (.016"x.022") FDA UDI

Identifiers

Catalog Number
50.62.151 FDA UDI
Primary DI / UDI-DI
07895742240783 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic archwire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Orthodontic archwire

Morelli by Dental Morelli Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic archwire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dental Morelli Ltda

Sources (1)

  • FDA UDI af18f95e-89e2-411b-8ff7-25ba5dbd4bca 35 fields · synced May 31, 2026