Fixture

GUDID 04046768001657

MAQUET GmbH

Operating/examination/treatment table headrest, reusable

• Primary Device ID: 04046768001657
• NIH Device Record Key: c9f3b1e8-915d-4a8e-a05d-0e9ea684661c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fixture
• Version Model Number: 100265A0
• Company DUNS: 315435859
• Company Name: MAQUET GmbH
• Device Count: 1
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046768001657 [Primary]

FDA Product Code

• BWN: TABLE AND ATTACHMENTS, OPERATING-ROOM

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: 2022-09-30
• Device Publish Date: 2022-09-22

Devices Manufactured by MAQUET GmbH

• 04046768148321 - Retrofit kit head fixation I: 2024-11-29
• 04046768148338 - Extension plate: 2024-11-29
• 04046768148345 - Extension plate: 2024-11-29
• 04046768148352 - Extension plate: 2024-11-29
• 04046768150973 - Extension plate: 2024-11-29
• 04046768151208 - Retrofit kit head fixation II: 2024-11-29
• 04046768145993 - Universal Remote Control: 2024-09-26
• 04046768148475 - Table width extension, long: 2024-06-11