MJM WOODTONE LINE

GUDID 00849229009773

M J M INTERNATIONAL CORPORATION

Hospital stretcher, manual

• Primary Device ID: 00849229009773
• NIH Device Record Key: 400a521a-b134-4853-aba0-c1877a9c0ad2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MJM WOODTONE LINE
• Version Model Number: WT920-B-MRI
• Company DUNS: 159688993
• Company Name: M J M INTERNATIONAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849229009773 [Primary]

FDA Product Code

• FPO: Stretcher, Wheeled

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: 2016-09-22

On-Brand Devices [MJM WOODTONE LINE]

• 00849229009773: WT920-B-MRI
• 00849229008288: WT910
• 00849229008271: WT910-HS
• 00849229008264: WT920-R