HMS PLUS

GUDID 00721902433719

RESERVOIR 31506 HMS

MEDTRONIC, INC.

Coagulation timer IVD

• Primary Device ID: 00721902433719
• NIH Device Record Key: b618667e-944e-415b-a927-25ad74d9a0d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HMS PLUS
• Version Model Number: 31506
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 100
• 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: true
• Serial Number: false
• 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

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00721902433719 [Primary]
GS1	70721902433718 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K894317

FDA Product Code

• JOX: ANALYZER, HEPARIN, AUTOMATED

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: 2016-04-28

On-Brand Devices [HMS PLUS]

• 00613994909404: RECONDITION HMS PLUS R30514AM
• 00681490512084: INSTRUMENT R30514 HMS PLUS RECON
• 00673978698793: INSTRUMENT 30514 HMS PLUS 110V EN
• 00721902433719: RESERVOIR 31506 HMS
• 00885074092904: INSTRUMENT E30514 HMS + EVAL UNIT
• 00763000158002: INST PKGD DOMESTIC 30514 HMS PLUS 511