INTL DMDM (STAND)-SPAIN

GUDID 00816711020677

INTL DMDM (STAND)-SPAIN

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit

• Primary Device ID: 00816711020677
• NIH Device Record Key: 87f1e19b-a77f-4059-b00f-414c99dc1d12
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTL DMDM (STAND)-SPAIN
• Version Model Number: 40151602SPAIN
• 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: true
• Manufacturing Date: false
• 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	00816711020677 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945722

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-08-31

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

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