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Aditek

FDA UDI

Class II (US FDA UDI)

by Aditek Do Brasil S/A

Identity

Trade Name
ADITEK FDA UDI
Generic Name
Self-ligating orthodontic bracket FDA UDI
Device Name
Bracket Ceramic Translux 018 Roth LR4 Hk -17°T 0°A w/1 FDA UDI
Model / Reference
05.02.0344 FDA UDI
Description
Bracket Ceramic Translux 018 Roth LR4 Hk -17°T 0°A w/1 FDA UDI

Identifiers

Catalog Number
05.02.0344 FDA UDI
Primary DI / UDI-DI
07899439223400 FDA UDI
FDA Product Code
NJM FDA UDI
GMDN Term
Self-ligating orthodontic bracket FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Self-ligating orthodontic bracket

Aditek by Aditek Do Brasil S/A — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-ligating orthodontic bracket.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3d1567d-3f32-4403-bf8e-5f1f75c5ae26 34 fields · synced May 30, 2026