Light guide

GUDID 04953170331718

"OCS5-LG OCS-500 LIGHT GUIDE"

OLYMPUS MEDICAL SYSTEMS CORP.

Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable

• Primary Device ID: 04953170331718
• NIH Device Record Key: 84e88a53-810c-4156-a4d4-20f2a1b249d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Light guide
• Version Model Number: OCS5-LG
• 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: 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170331718 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K852980

FDA Product Code

• HEX: COLPOSCOPE (AND COLPOMICROSCOPE)
• PTZ: Colposcope (And Colpomicroscope), Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-21

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