Pipette tip 70.3070.275

GUDID 04066916031985

Sarstedt Aktiengesellschaft & Co.KG

User-induced pipette
Primary Device ID04066916031985
NIH Device Record Key31ec837f-1067-4932-b250-70e00603f850
Commercial Distribution StatusIn Commercial Distribution
Brand NamePipette tip
Version Model Number70.3070.275
Catalog Number70.3070.275
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count480
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104066916031985 [Unit of Use]
GS104066916031992 [Primary]

FDA Product Code

JRCMicro Pipette

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-14
Device Publish Date2025-04-04

On-Brand Devices [Pipette tip]

0406691602210570.3070
0406691602346170.3070.255
0406691603202970.3070.210
0406691603198570.3070.275
0406691603184870.3070.375
0406691602513770.3070.355
0406691602434570.3070.305
0406691603170170.3070.110

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.