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Aditek

FDA UDI

Class I (US FDA UDI)

by Aditek Do Brasil S/A

Identity

Trade Name
ADITEK FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
Kit 5x5 EasyClip+ Passive 022 MBT Maxillary Hk 3,4,5 w/10 FDA UDI
Model / Reference
05.21.0893 FDA UDI
Description
Kit 5x5 EasyClip+ Passive 022 MBT Maxillary Hk 3,4,5 w/10 FDA UDI

Identifiers

Catalog Number
05.21.0893 FDA UDI
Primary DI / UDI-DI
07899439207776 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic bracket, metal 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Orthodontic bracket, metal

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

Similar devices

Also classified as Orthodontic bracket, metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df66b9ea-ca99-4794-8621-ee29f74627b1 34 fields · synced May 30, 2026