Inoris Medical Sp. z o.o.

GUDID 05902596226077

Disposable biteblock for adults

INORIS MEDICAL SP Z O O

Seizure bite block

• Primary Device ID: 05902596226077
• NIH Device Record Key: e03a4817-7a6f-47ac-93a0-7597f40ed771
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inoris Medical Sp. z o.o.
• Version Model Number: IM-10
• Company DUNS: 522725233
• Company Name: INORIS MEDICAL SP Z O O
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: false
• 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	05902596226077 [Primary]
GS1	05902596226992 [Unit of Use]

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: 2021-02-11
• Device Publish Date: 2021-02-03

On-Brand Devices [Inoris Medical Sp. z o.o.]

• 05902596226060: Biteblocks for adults
• 05902596226428: IM-200 Scanhead Protection Cover
• 05902596226121: IM-20 Clip-on Biteguard
• 05902596226077: Disposable biteblock for adults