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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 palate expander/teeth aligner, bonded FDA UDI
Device Name
Expansion Screw Palatal Split - Expansion 11mm FDA UDI
Model / Reference
99.65.004 FDA UDI
Description
Expansion Screw Palatal Split - Expansion 11mm FDA UDI

Identifiers

Catalog Number
99.65.004 FDA UDI
Primary DI / UDI-DI
07895742296636 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic palate expander/teeth aligner, bonded 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
MRI Safety
MR Conditional FDA UDI

Category: Orthodontic palate expander/teeth aligner, bonded

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

Similar devices

Also classified as Orthodontic palate expander/teeth aligner, bonded.

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 a396a4d6-2754-4c55-9cec-95d08a0b4a4b 35 fields · synced May 30, 2026