INTL DMDM (STAND)-SPAIN 91525179

GUDID 00816711023845

40151602 Digital MDM, 30%, Spain

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit

• Primary Device ID: 00816711023845
• NIH Device Record Key: 5a7f9b21-cf34-4d53-9d1b-d9b9082b2d9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTL DMDM (STAND)-SPAIN
• Version Model Number: 91525179
• Catalog Number: 91525179
• Company DUNS: 004175550
• Company Name: PARKER-HANNIFIN CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816711023845 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K884879

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

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: 2023-09-13
• Device Publish Date: 2023-09-05

On-Brand Devices [INTL DMDM (STAND)-SPAIN]

• 00816711020677: INTL DMDM (STAND)-SPAIN
• 00816711023845: 40151602 Digital MDM, 30%, Spain