Single Use Rotatable Clip Fixing Device

GUDID 14953170353120

Single Use Rotatable Clip Fixing Device

OLYMPUS MEDICAL SYSTEMS CORP.

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• Primary Device ID: 14953170353120
• NIH Device Record Key: 10babad2-6ffa-4577-a4dd-03531af22474
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Use Rotatable Clip Fixing Device
• Version Model Number: HX-201UR-135
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170353123 [Primary]
GS1	14953170353120 [Package]; Contains: 04953170353123; Package: [5 Units]; In Commercial Distribution
GS1	54953170353128 [Package]; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• MND: Ligator, esophageal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [Single Use Rotatable Clip Fixing Device]

• 14953170353175: Single Use Rotatable Clip Fixing Device
• 14953170353168: Single Use Rotatable Clip Fixing Device
• 14953170353151: Single Use Rotatable Clip Fixing Device
• 14953170353144: HX-201LR-135L
• 14953170353137: Single Use Rotatable Clip Fixing Device
• 14953170353120: Single Use Rotatable Clip Fixing Device
• 14953170353113: Single Use Rotatable Clip Fixing Device
• 14953170353106: Single Use Rotatable Clip Fixing Device
• 14953170353090: Single Use Rotatable Clip Fixing Device
• 14953170254885: HX-201YR-135
• 14953170206976: HX-201UR-135L
• 14953170206952: HX-201UR-135L
• 14953170206921: HX-201LR-135L
• 14953170206907: HX-201LR-135L
• 14953170193047: HX-201UR-135
• 14953170193023: HX-201UR-135
• 14953170192996: HX-201LR-135
• 14953170192972: HX-201LR-135
• 14953170462549: HX-201UR-135L
• 14953170462488: HX-201LR-135L
• 14953170462426: HX-201UR-135
• 14953170462396: HX-201LR-135