MJM 900 SERIES GURNEY

GUDID 00849229003726

M J M INTERNATIONAL CORPORATION

Hospital stretcher, manual

• Primary Device ID: 00849229003726
• NIH Device Record Key: b523c317-5e71-4207-bd90-a8bbcf292ce7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MJM 900 SERIES GURNEY
• Version Model Number: 910-B
• Company DUNS: 159688993
• Company Name: M J M INTERNATIONAL 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: 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	00849229003726 [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 900 SERIES GURNEY]

• 00849229009766: 930
• 00849229009759: 900-HAZMAT
• 00849229009742: 920-R-MRI
• 00849229009735: 920-P-MRI
• 00849229009728: 920-FD-PAD
• 00849229009711: 920-B-MRI
• 00849229009704: 915-PAD
• 00849229009698: 915-B-MRI
• 00849229009681: 915-MRI
• 00849229009674: 911-B-MRI
• 00849229009667: 911
• 00849229009650: 910-B-HS
• 00849229009643: 910-P
• 00849229009209: 951
• 00849229009186: 900-ATS
• 00849229009155: 911-MRI
• 00849229009148: 915-24
• 00849229003818: 920-R
• 00849229003801: 920-P
• 00849229003771: 920-MRI
• 00849229003740: 920
• 00849229003733: 910-DB
• 00849229003726: 910-B
• 00849229001791: 910-HS
• 00849229001357: 915
• 00849229009131: E915
• 00897074002166: 910