Primary Device ID | 04046768150973 |
NIH Device Record Key | 21da701d-c481-4fdb-aa46-65baa1bcae66 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Extension plate |
Version Model Number | 116033FC |
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 | 04046768150973 [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 | 2024-11-29 |
Device Publish Date | 2024-11-21 |
04046768138360 | 116032DC |
04046768137752 | N.A. |
04046768137745 | 116032BC |
04046768134638 | 116032FC |
04046768134621 | 116032AC |
04046768089037 | 113131FC |
04046768089013 | 113131BC |
04046768040922 | 118046A0 |
04046768031852 | 118032F0 |
04046768031838 | 118032A0 |
04046768000292 | 10035200 |
04046768150973 | 116033FC |
04046768148352 | 116033GC |
04046768148345 | 116033BC |
04046768148338 | 116033DC |