Primary Device ID | 16976299950108 |
NIH Device Record Key | 8a7c8373-fd34-49f4-9a0c-0fc83bec155b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SMARTBEAM |
Version Model Number | ZS712L |
Company DUNS | 706528439 |
Company Name | Beijing Smartbeam Technology Co., LTD |
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 | true |
Serial Number | false |
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 | 16976299950108 [Primary] |
ITY | Assembly, Tube Housing, X-Ray, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-14 |
Device Publish Date | 2023-06-06 |
16976299950122 | ZS802B |
16976299950085 | ZS632B |
16976299950139 | ZS802L |
16976299950115 | ZS752B |
16976299950108 | ZS712L |
16976299950092 | ZS702L |
16976299950078 | ZS602L |
16976299950061 | ZS502L |
16976299950054 | ZS502B |
16976299950047 | ZS402L |
16976299950030 | ZS352C |
16976299950023 | ZS352B |
16976299950016 | ZS302B |
06976299950279 | ZS502L/H580C |
06976299950262 | ZS802L/H560A |
06976299950255 | ZS802B/H601A |
06976299950248 | ZS752B/H425A |
06976299950231 | ZS712L/H485B |
06976299950224 | ZS702L/H847B |
06976299950217 | ZS632B/H847A |
06976299950200 | ZS602L/H560B |
06976299950194 | ZS502L/H580A |
06976299950187 | ZS502B/H590A |
06976299950170 | ZS402L/H493A |
06976299950163 | ZS352C/H485A |
06976299950156 | ZS352B/H498A |
06976299950149 | ZS302B/H580B |