Reflex Coil Spring

GUDID 00192029016022

Aesthetic Open Coil Spring Medium Force

TP ORTHODONTICS INC

Orthodontic wire

• Primary Device ID: 00192029016022
• NIH Device Record Key: 1fe2ac79-6969-410c-92f4-36801b666a33
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reflex Coil Spring
• Version Model Number: 210-501W
• Company DUNS: 005432299
• Company Name: TP ORTHODONTICS INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192029016022 [Primary]

FDA Product Code

• DZC: WIRE, ORTHODONTIC

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-23
• Device Publish Date: 2021-03-15

On-Brand Devices [Reflex Coil Spring]

• 00192029016091: Double Coil Spring
• 00192029016084: Closed Coil Spring Heavy
• 00192029016077: Closed Coil Spring Medium
• 00192029016060: Closed Coil Spring Light
• 00192029016053: Double Coil Spring
• 00192029016039: Open Coil Spring Heavy Force
• 00192029016022: Aesthetic Open Coil Spring Medium Force
• 00192029016015: Open Coil Spring Medium Force
• 00192029016008: Open Coil Spring Light Force