Teleflex

GUDID B504LG41501200

Provision

Rigid intubation laryngoscope, single-use

• Primary Device ID: B504LG41501200
• NIH Device Record Key: 3fecb661-fd69-44ed-86cb-77fbf3f7b4ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Teleflex
• Version Model Number: 4150120
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504LG41501200 [Primary]

FDA Product Code

• CCW: Laryngoscope, Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-05
• Device Publish Date: 2024-03-28

On-Brand Devices [Teleflex]

• B504GS5025050: 502505
• B504OMKM481400: KM48-140
• B504GS5025070: 502507
• B504GS1053000000250: 105300-000025
• B504GS1216050: 12-1605
• B504LG41501400: 4150140
• B504LG41501300: 4150130
• B504LG41501200: 4150120
• B504LG41500200: 4150020
• B504GS1653480: 16-5348
• B504GS1812230: 18-1223
• B504LG0045500030: 004550003
• B504LG41500150: 4150015
• B504OMKM481320: KM48-132