INORIS MEDICAL

GUDID 05902596226008

INORIS MEDICAL SP Z O O

Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block Seizure bite block

• Primary Device ID: 05902596226008
• NIH Device Record Key: 3dbb2577-2df8-4d19-93c5-971a0eef27fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INORIS MEDICAL
• Version Model Number: IM-50
• Company DUNS: 522725233
• Company Name: INORIS MEDICAL SP Z O O
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	05902596226008 [Primary]

FDA Product Code

• MNK: Endoscopic Bite Block

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: 2021-01-20
• Device Publish Date: 2021-01-12

On-Brand Devices [INORIS MEDICAL]

• 05902596226008: IM-50
• 05902596226367: IM-60 Adult Biteguard