Primary Device ID | 04038917112529 |
NIH Device Record Key | cb2f2305-ab4f-4f77-a67e-fec7e35b1c59 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | tube with screw cap 7ml, 82x13mm, PP |
Version Model Number | 60.550.049 |
Catalog Number | 60.550.049 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 100 |
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 | 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 | |
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 | 04038917112529 [Unit of Use] |
GS1 | 04038917188852 [Primary] |
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 | 2023-07-31 |
Device Publish Date | 2023-07-22 |
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04066916031848 - Pipette tip | 2025-04-14 |
04066916031985 - Pipette tip | 2025-04-14 |
04066916032029 - Pipette tip | 2025-04-14 |
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04066916022907 - Pipette tip 1250 µl XL | 2025-02-28 |