Primary Device ID | 04038917194372 |
NIH Device Record Key | 29e947de-d4db-400c-b2e2-cb198f9cf223 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micro tube 0.5ml with cap |
Version Model Number | 72.730.008 |
Catalog Number | 72.730.008 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 500 |
DM Exempt | true |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04038917119306 [Primary] |
GS1 | 04038917194372 [Unit of Use] |
NNK | CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-08 |
Device Publish Date | 2022-11-30 |
04038917390811 | 72.730.407 |
04038917194747 | 72.733.001 |
04038917194372 | 72.730.008 |
04038917194365 | 72.730.007 |
04038917165990 | 72.730 |
04038917994507 | 72.730.309 |
04038917994330 | 72.730.307 |
04038917994040 | 72.730.300 |