Primary Device ID | 04038917165204 |
NIH Device Record Key | 75cd180e-bf73-4dbc-920e-4950f6a77835 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 3.5ml, 92x13 (round), PP |
Version Model Number | 62.617 |
Catalog Number | 62.617 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 100 |
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 | 04038917082921 [Primary] |
GS1 | 04038917165204 [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 |
04038917932042 | 60.617.202 |
04038917898614 | 60.617.201 |
04038917191036 | 60.617.010 |
04038917165204 | 62.617 |