TRACHEAL INTUBATION FIBERSCOPE

GUDID 04953170061998

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible fibreoptic intubation laryngoscope

• Primary Device ID: 04953170061998
• NIH Device Record Key: 15887494-3f30-4bb7-b577-14e3a14a9c23
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRACHEAL INTUBATION FIBERSCOPE
• Version Model Number: OLYMPUS LF-GP
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• Device Count: 1
• DM Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170061998 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K981543

FDA Product Code

• EOQ: BRONCHOSCOPE (FLEXIBLE OR RIGID)

Sterilization

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

[04953170061998]

Ethylene Oxide;High-level Disinfectant

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-08
• Device Publish Date: 2016-09-21

On-Brand Devices [TRACHEAL INTUBATION FIBERSCOPE]

• 04953170340215: LF-GP TRACHEAL INTUBATION FIBE RSCOPE-PO
• 04953170340192: LF-DP TRACHEAL INTUBATION FIBE RSCOPE-PO
• 04953170136856: OLYMPUS LF-DP
• 04953170136825: LF-TP TRACHEAL INTUBATION FIBE RSCOPE-PO
• 04953170061998: OLYMPUS LF-GP
• 04953170452932: OLYMPUS LF-P