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Mirabay

FDA UDI

Class I (US FDA UDI)

by Mirabay Orthodontics Corporation

Identity

Trade Name
MIRABAY FDA UDI
Generic Name
Orthodontic inter-arch elastic band FDA UDI
Device Name
HERO N LATEX AMBER 1/8 INCH MEDIUM 4.5 OZ ELASTICS POUCH 50PKS FDA UDI
Model / Reference
4NBL-012 FDA UDI
Description
HERO N LATEX AMBER 1/8 INCH MEDIUM 4.5 OZ ELASTICS POUCH 50PKS FDA UDI

Identifiers

Catalog Number
4NBL-012 FDA UDI
Primary DI / UDI-DI
05061075025256 FDA UDI
FDA Product Code
ECI 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

Yes

FDA UDI

Category: Orthodontic inter-arch elastic band

Mirabay by Mirabay Orthodontics Corporation — 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

Sources (1)

  • FDA UDI ea234975-54d1-4074-8454-638fadf8a2b0 35 fields · synced Jun 6, 2026