DALTON OVERBED TABLE

GUDID 00815027011362

OVERBED TABLE, NON-TILT

DALTON MEDICAL CORPORATION

Overbed table

• Primary Device ID: 00815027011362
• NIH Device Record Key: dcad3d9a-d115-4a74-9b98-1b4aafc8b965
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DALTON OVERBED TABLE
• Version Model Number: B-T3015P
• Company DUNS: 874709348
• Company Name: DALTON MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00815027011362 [Primary]

FDA Product Code

• INW: Table, Mechanical

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: 2020-05-11
• Device Publish Date: 2020-05-01

On-Brand Devices [DALTON OVERBED TABLE]

• 00815027011379: OVERBED TABLE, TILT,
• 00815027011362: OVERBED TABLE, NON-TILT