Primary Device ID | 04038917432245 |
NIH Device Record Key | 7ee423ee-b8c3-4269-9896-b3db19f48340 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pipette tip 1250 µl XL |
Version Model Number | 70.3060.110 |
Catalog Number | 70.3060.110 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 1920 |
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 | 04038917432238 [Primary] |
GS1 | 04038917432245 [Unit of Use] |
JRC | MICRO PIPETTE |
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 |
04038917434652 | 70.3060 |
04038917432481 | 70.3060.305 |
04038917432399 | 70.3060.205 |
04038917432368 | 70.3060.210 |
04038917432337 | 70.3060.200 |
04038917432245 | 70.3060.110 |
04038917432214 | 70.3060.100 |
04066916023065 | 70.3070.200 |
04066916022907 | 70.3070.205 |