Primary Device ID | 04038917188159 |
NIH Device Record Key | e8c8d226-45a5-460f-88b5-567b0dd98a17 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 30ml, 107x25mm, PP |
Version Model Number | 62.543.001 |
Catalog Number | 62.543.001 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 50 |
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 | 04038917111638 [Primary] |
GS1 | 04038917188159 [Unit of Use] |
KDT | CONTAINER, SPECIMEN MAILER AND STORAGE, STERILE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-08 |
Device Publish Date | 2022-11-30 |
04038917188234 | 62.543.030 |
04038917188159 | 62.543.001 |
04038917164641 | 62.543 |