DIGITAL MDM 30% GERMANY 91525178

GUDID 00816711023838

40151602 Digital MDM, 30%, Germany, Straight Fittings

PARKER-HANNIFIN CORPORATION

Inhalational analgesia unit

• Primary Device ID: 00816711023838
• NIH Device Record Key: 48d0e0fe-94d8-415f-a5d1-1b8e1bd02de2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIGITAL MDM 30% GERMANY
• Version Model Number: 91525178
• Catalog Number: 91525178
• 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	00816711023838 [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

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