Primary Device ID | 00840682146210 |
NIH Device Record Key | 650b003b-eff1-4255-ad22-0a1b67363fd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Discovery |
Version Model Number | XR656 |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682146210 [Primary] |
KPR | System, x-ray, stationary |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-22 |
Device Publish Date | 2019-08-14 |
00840682146210 | XR656 |
00840682138598 | XR656 HD |
00840682118699 | RT |
00840682115322 | XR656 |