VAMA VMA

GUDID 18435194316252

VAMA INTUBATION CANNULA FOR FIBROSCOPIC INTUBATION

AJL OPHTHALMIC SA

Oropharyngeal airway, single-use

• Primary Device ID: 18435194316252
• NIH Device Record Key: d72a6243-b42f-44e2-a06b-4cfbc20c6925
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VAMA
• Version Model Number: VMA
• Catalog Number: VMA
• Company DUNS: 472925262
• Company Name: AJL OPHTHALMIC SA
• Device Count: 10
• DM Exempt: false
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com
• Phone: +34945298256
• Email: evalarra@ajlsa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08435194316255 [Unit of Use]
GS1	18435194316252 [Primary]

FDA Product Code

• CAE: Airway, Oropharyngeal, Anesthesiology

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-07
• Device Publish Date: 2023-07-28