DARCO® AirTraveler™ Walker AT4

GUDID 20609271989454

XL Black High version

DARCO INTERNATIONAL, INC.

Inflatable extremity splint

• Primary Device ID: 20609271989454
• NIH Device Record Key: 75143037-e733-409c-b9ca-8dfabc215bde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DARCO® AirTraveler™ Walker
• Version Model Number: AT4
• Catalog Number: AT4
• Company DUNS: 184231298
• Company Name: DARCO INTERNATIONAL, 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: true
• Expiration Date: false
• 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	00609271989450 [Primary]
GS1	10609271989457 [Package]; Contains: 00609271989450; Package: Box [4 Units]; In Commercial Distribution
GS1	20609271989454 [Package]; Contains: 00609271989450; Package: Case [12 Units]; In Commercial Distribution

FDA Product Code

• FZF: SPLINT, EXTREMITY, INFLATABLE, EXTERNAL

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: 2023-02-16
• Device Publish Date: 2023-02-08

On-Brand Devices [DARCO® AirTraveler™ Walker]

• 20609271999453: XL Black Low version
• 10609271999357: L Black Low version
• 20609271999255: M Black Low version
• 20609271999156: S Black Low version
• 10609271999050: XS Black Low version
• 20609271989454: XL Black High version
• 10609271989358: L Black High version
• 20609271989256: M Black High version
• 10609271989150: S Black High version
• 10609271989051: XS Black High version