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Enchanted Series

FDA UDI

Class I (US FDA UDI)

by G&H Wire Company, Inc.

Identity

Trade Name
ENCHANTED SERIES FDA UDI
Generic Name
Orthodontic inter-arch elastic band FDA UDI
Device Name
ENCHANTED SER AMB 3/16 MD ELAST FDA UDI
Model / Reference
36MDAM FDA UDI
Description
ENCHANTED SER AMB 3/16 MD ELAST FDA UDI

Identifiers

Primary DI / UDI-DI
10190886033364 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

Yes

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

Enchanted Series by G&H Wire Company, Inc. — 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 204ebc73-b942-4624-b916-b1a60932db54 34 fields · synced Jun 8, 2026