INTL DMDM (STAND)-SPAIN 91525179

GUDID 00816711023845

40151602 Digital MDM, 30%, Spain

PARKER-HANNIFIN CORPORATION

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