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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 inter-arch elastic band FDA UDI
Device Name
Telescopic Tube for wires up to Ø0,80mm FDA UDI
Model / Reference
30.40.030 FDA UDI
Description
Telescopic Tube for wires up to Ø0,80mm FDA UDI

Identifiers

Catalog Number
30.40.030 FDA UDI
Primary DI / UDI-DI
07895742168346 FDA UDI
FDA Product Code
ECN FDA UDI
GMDN Term
Orthodontic inter-arch elastic band 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 inter-arch elastic band

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

Similar devices

Also classified as Orthodontic inter-arch elastic band.

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 3cd02ec2-5c9e-4cd9-b209-d169051d6cbb 35 fields · synced May 29, 2026