APPUI-TETE REGLABLE AMOVIBLE/ ADJUSTABLE HEADREST

GUDID 03664560000145

SARL VIPAMAT

Wheelchair/chair/stander headrest

• Primary Device ID: 03664560000145
• NIH Device Record Key: 082af516-9d41-4a16-892c-b4178e79d108
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: APPUI-TETE REGLABLE AMOVIBLE/ ADJUSTABLE HEADREST
• Version Model Number: 0008-00-04
• Company DUNS: 264013397
• Company Name: SARL VIPAMAT
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03664560000145 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051709

FDA Product Code

• IQC: Wheelchair, Special Grade

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-03-05
• Device Publish Date: 2017-05-26

On-Brand Devices [APPUI-TETE REGLABLE AMOVIBLE/ ADJUSTABLE HEADREST]

• 03664560000176: 0008-00-05
• 03664560000145: 0008-00-04