CONNECTING TUBE

GUDID 04953170234026

OLYMPUS MEDICAL SYSTEMS CORP.

Luer/non-ISO80369-standardized linear connector, reusable

• Primary Device ID: 04953170234026
• NIH Device Record Key: d5fc55ca-7c1a-47ce-80e0-c2ad2f06ee93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONNECTING TUBE
• Version Model Number: MAJ-1513
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Device Issuing Agency	Device ID
GS1	04953170234026 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103264

FDA Product Code

• FEB: ACCESSORIES, CLEANING, FOR ENDOSCOPE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-09-21

On-Brand Devices [CONNECTING TUBE]

• 04953170350474: MAJ-2124
• 04953170332890: MAJ-1969
• 04953170329623: MAJ-1971
• 04953170299353: MAJ-1904
• 04953170258626: MAJ-1764
• 04953170234064: MAJ-1517
• 04953170234057: MAJ-1516
• 04953170234040: MAJ-1515
• 04953170234033: MAJ-1514
• 04953170234026: MAJ-1513
• 04953170234019: MAJ-1512
• 04953170234002: MAJ-1511
• 04953170233982: MAJ-1508
• 04953170233975: MAJ-1505
• 04953170233968: MAJ-1504
• 04953170233951: MAJ-1503
• 04953170233937: MAJ-1500
• 04953170409820: MAJ-2358
• 04953170312670: MAJ-1838
• 04953170312663: MAJ-1837
• 04953170404207: MAJ-2330
• 04953170404184: MAJ-2138
• 04953170404146: MAJ-2119
• 04953170404139: MAJ-2118
• 04953170404122: MAJ-2117
• 04953170404115: MAJ-2116
• 04953170404108: MAJ-2115
• 04953170404092: MAJ-2114
• 04953170404085: MAJ-2113
• 04953170404078: MAJ-2112
• 04953170404061: MAJ-2111
• 04953170404054: MAJ-2110
• 04953170312656: MAJ-1836
• 04953170438349: MAJ-2358
• 04953170437861: MAJ-1969
• 04953170437854: MAJ-1971
• 04953170437694: MAJ-1764
• 04953170437687: MAJ-1517
• 04953170437670: MAJ-1516
• 04953170437663: MAJ-1515
• 04953170437656: MAJ-1514
• 04953170437649: MAJ-1513
• 04953170437632: MAJ-1512
• 04953170437625: MAJ-1511
• 04953170437601: MAJ-1508
• 04953170437595: MAJ-1505
• 04953170437588: MAJ-1504
• 04953170437571: MAJ-1503
• 04953170437564: MAJ-1500