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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 archwire FDA UDI
Device Name
OPTIMAL SYMMETRY ARCHWIRE TRANS THERM LF 0.014 L1 PK10 FDA UDI
Model / Reference
515-0003 FDA UDI
Description
OPTIMAL SYMMETRY ARCHWIRE TRANS THERM LF 0.014 L1 PK10 FDA UDI

Identifiers

Catalog Number
515-0003 FDA UDI
Primary DI / UDI-DI
05061075029094 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic archwire 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic archwire

Mirabay by Mirabay Orthodontics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic archwire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b9e58422-3dd0-4405-8289-804f876b4362 35 fields · synced Jun 1, 2026