ORLIMAN

GUDID 08435025922129

ORLIMAN S.L.U.

Abdominal hernia truss, reusable

• Primary Device ID: 08435025922129
• NIH Device Record Key: 4118aacf-9518-471e-827d-1a96d851369c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ORLIMAN
• Version Model Number: I-112#8
• Company DUNS: 479135550
• Company Name: ORLIMAN S.L.U.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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	08435025922129 [Primary]

FDA Product Code

• EXN: Support, Hernia

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: 2023-08-09
• Device Publish Date: 2023-08-01

On-Brand Devices [ORLIMAN]

• 08435025922129: I-112#8
• 08435025919693: D-111#10
• 08435025919686: D-111#9
• 08435025919679: D-111#8
• 08435025914858: B-110#12
• 08435025914841: B-110#11
• 08435025914834: B-110#10
• 08435025914827: B-110#9
• 08435025914810: B-110#8
• 08435025922150: I-112#11
• 08435025922143: I-112#10
• 08435025919709: D-111#11