← Back to catalogue

Glide Chain Elastic

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
GLIDE CHAIN ELASTIC FDA UDI
Generic Name
Orthodontic inter-bracket elastic chain FDA UDI
Device Name
GLIDE CHAIN ELASTIC SHORT BURGUNDY 15' FDA UDI
Model / Reference
300-322 FDA UDI
Description
GLIDE CHAIN ELASTIC SHORT BURGUNDY 15' FDA UDI

Identifiers

Catalog Number
300-322 FDA UDI
Primary DI / UDI-DI
D9093003220 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

Glide Chain Elastic by Ortho Arch Company Inc — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b5116f25-3821-46de-95e8-0688fcd82ecf 34 fields · synced Jun 6, 2026