DIERS postura

GUDID 04260242060194

DIERS International GmbH

Radiological video camera patient positioning/tracking system

• Primary Device ID: 04260242060194
• NIH Device Record Key: 07c16c9a-9cef-40bb-9d0d-0fb02243f43d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIERS postura
• Version Model Number: n/a
• Company DUNS: 499189983
• Company Name: DIERS International GmbH
• 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: false
• Lot Batch: true
• Serial Number: true
• 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	04260242060194 [Primary]

FDA Product Code

• KQX: Goniometer, Ac-Powered

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: 2023-06-12
• Device Publish Date: 2023-06-02

Devices Manufactured by DIERS International GmbH

• 04260242060019 - DIERS formetric: 2023-06-12
• 04260242060064 - DIERS leg axis: 2023-06-12
• 04260242060071 - DIERS pedoscan: 2023-06-12
• 04260242060101 - DIERS statico: 2023-06-12
• 04260242060118 - DIERS myoline: 2023-06-12
• 04260242060125 - DIERS leg axis lateral: 2023-06-12
• 04260242060132 - DIERS pedogait: 2023-06-12
• 04260242060163 - DIERS leg axis: 2023-06-12