Primary Device ID | 04038917274159 |
NIH Device Record Key | 8850cbcd-2d18-4a1e-acca-727e0b4d5173 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FB Tube 2.5ml, 75x13 (round) |
Version Model Number | 60.614.010 |
Catalog Number | 60.614.010 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 1000 |
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 | 04038917274159 [Unit of Use] |
GS1 | 04038917353182 [Primary] |
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 |
04038917418249 | 60.614.027 |
04038917418218 | 60.614.026 |
04038917418188 | 60.614.025 |
04038917418157 | 60.614.024 |
04038917274159 | 60.614.010 |
04038917349772 | 60.614.065 |
04038917280051 | 60.614.015 |
04038917346818 | FB tube 2.5ml, 75x13 (round) |