Hillrom

GUDID 00887761975354

WAVE Clinical Platform 1.7

HILL-ROM, INC.

Medical equipment clinical data interfacing software

• Primary Device ID: 00887761975354
• NIH Device Record Key: 0c99725a-09cb-4d1f-9426-1b3b17849dc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hillrom
• Version Model Number: 1.7
• Company DUNS: 004245668
• Company Name: HILL-ROM, INC.
• 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: 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)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hill-rom.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887761975354 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171056

FDA Product Code

• MWI: Monitor, physiological, patient (without arrhythmia detection or alarms)

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: 2022-10-28
• Device Publish Date: 2022-10-20

Devices Manufactured by HILL-ROM, INC.

• 00887761976542 - Experience Pod: 2025-01-28 Experience Pod
• 00887761007710 - Centrella™ Surface: 2024-12-05 CENTRELLA® MAX SURFACE
• 00887761007727 - Centrella™ Surface: 2024-12-05 CENTRELLA® MAX SURFACE WITH X-RAY
• 00887761007734 - Centrella™ Surface: 2024-12-05 CENTRELLA® MAX SURFACE
• 00887761007741 - Centrella™ Surface: 2024-12-05 CENTRELLA® MAX, NARROW, RENTAL
• 00887761007758 - Centrella™ Surface: 2024-12-05 CENTRELLA® MAX, WIDE, RENTAL
• 00887761007765 - Centrella™ Surface: 2024-12-05 CENTRELLA AIR, REPLACEMENT, X-RAY SLEEVE, TOP COVER
• 00887761966819 - Centrella™ Surface: 2024-09-30 Centrella Air, Replacement, X-Ray, sleeve, Top Cover