MECRON Hip-Compression U: 105-125 cm 38-052

GUDID 10609271950051

L White right

DARCO INTERNATIONAL, INC.

Hip orthosis

• Primary Device ID: 10609271950051
• NIH Device Record Key: c73c345d-f2c2-4a66-92dc-a4fe2ba1aafb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MECRON Hip-Compression U: 105-125 cm
• Version Model Number: 38-052
• Catalog Number: 38-052
• 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	00609271950054 [Primary]
GS1	10609271950051 [Package]; Contains: 00609271950054; Package: Box [12 Units]; In Commercial Distribution

FDA Product Code

• IQI: ORTHOSIS, LIMB BRACE

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: 2023-02-22
• Device Publish Date: 2023-02-14

On-Brand Devices [MECRON Hip-Compression U: 105-125 cm]

• 10609271950068: L White left
• 10609271950051: L White right