Arion Proth-Pro Arm

GUDID 08717127931767

Donning aid for transhumeral or transradial prostheses

Arion Holding B.V.

Stump sock

• Primary Device ID: 08717127931767
• NIH Device Record Key: 3a38973d-2a0c-40fb-8ba0-32c104b8e8bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arion Proth-Pro Arm
• Version Model Number: Medium
• Company DUNS: 489495862
• Company Name: Arion Holding B.V.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	08717127931767 [Primary]

FDA Product Code

• IPM: Cover, Limb

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: 2025-01-21
• Device Publish Date: 2025-01-13

On-Brand Devices [Arion Proth-Pro Arm]

• 08717127931798: Donning aid for transhumeral or transradial prostheses
• 08717127931767: Donning aid for transhumeral or transradial prostheses
• 08717127931736: Donning aid for transhumeral or transradial prostheses