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3M™ AlastiK™

FDA UDI

Class I (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
3M™ AlastiK™ FDA UDI
Generic Name
Orthodontic inter-bracket elastic chain FDA UDI
Device Name
3M™ AlastiK™ B Modules, 406-024, B-1, Clear, Heavy, 100/Pk FDA UDI
Model / Reference
406-024 FDA UDI
Description
3M™ AlastiK™ B Modules, 406-024, B-1, Clear, Heavy, 100/Pk FDA UDI

Identifiers

Catalog Number
406-024 FDA UDI
Primary DI / UDI-DI
00652221073815 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic inter-bracket elastic chain 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-bracket elastic chain

3M™ AlastiK™ by 3m Unitek Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic inter-bracket elastic chain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72ac16d3-995c-45bb-b62e-62a3b8a2046d 35 fields · synced May 30, 2026