Centrella™ Bed

GUDID 00887761999961

Hospital Bed

HILL-ROM, INC.

Basic electric hospital bed

• Primary Device ID: 00887761999961
• NIH Device Record Key: e58f58f4-973a-4cde-9c6e-5417fc6d7228
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centrella™ Bed
• Version Model Number: P7900A
• Company DUNS: 004245668
• Company Name: HILL-ROM, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887761999961 [Primary]

FDA Product Code

• FNL: BED, AC-POWERED ADJUSTABLE HOSPITAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-06-29

On-Brand Devices [Centrella™ Bed]

• 00887761999961: Hospital Bed
• 00887761985162: Hospital Bed