Primary Device ID | 00195278527455 |
NIH Device Record Key | 4a180595-1cec-4d40-851e-f0f4c13a947e |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 9999666 |
Catalog Number | 9999666 |
Company DUNS | 654659689 |
Company Name | Hangwei GE Medical Systems Co., Ltd. |
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 | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00195278527455 [Primary] |
IZZ | Table, radiographic, non-tilting, powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-29 |
Device Publish Date | 2022-07-21 |
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00195278788665 - Revolution Apex | 2024-01-03 Revolution Apex Select with Plus Edition - Designated System Medical Device |
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00195278713759 - NA | 2023-09-26 Galaxy 2.0 Wall Stand |
00195278713766 - NA | 2023-09-26 Value Fixed Table |
00195278686718 - Revolution | 2023-06-30 Revolution Maxima CT designated medical device |