Primary Device ID | 04046768001589 |
NIH Device Record Key | cb2f4c22-c9b2-4c03-819a-968c40f12a64 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Support bar |
Version Model Number | 100218A0 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 04046768001589 [Primary] |
BWN | TABLE AND ATTACHMENTS, OPERATING-ROOM |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-30 |
Device Publish Date | 2022-09-22 |
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04046768146044 - Carbon Fiber Table Top | 2025-02-04 |
04046768146051 - Carbon Fiber Table Top | 2025-02-04 |
04046768146853 - Joystick | 2025-02-04 |
04046768001954 - Femur counter traction post table top | 2025-01-20 |
04046768148321 - Retrofit kit head fixation I | 2024-11-29 |
04046768148338 - Extension plate | 2024-11-29 |
04046768148345 - Extension plate | 2024-11-29 |