Primary Device ID | 04046768040977 |
NIH Device Record Key | 751bb8c2-c87b-43f6-82c7-3c10976071e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pair of leg plates |
Version Model Number | 118054G0 |
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 | 04046768040977 [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 |
04046768138353 | 116050DC |
04046768137738 | 116050GC |
04046768137721 | 116050BC |
04046768134669 | 116050FC |
04046768134652 | 116050AC |
04046768133303 | 100742AC |
04046768103153 | 115064E0 |
04046768075849 | 115073DC |
04046768073807 | 115073BC |
04046768073296 | 113373BC |
04046768073036 | 113373FC |
04046768040977 | 118054G0 |
04046768032033 | 118054F0 |
04046768032026 | 118054B0 |
04046768032002 | 118054A0 |
04046768031203 | 115064B0 |
04046768030183 | 111850F0 |
04046768003637 | 115064D0 |
04046768002982 | 113353FC |
04046768002975 | 113353BC |
04046768002395 | 111850B0 |
04046768149564 | 111861FC |
04046768149557 | 111861BC |