Primary Device ID | 20888937014062 |
NIH Device Record Key | 097807c1-04d5-4e05-81ee-17c6df2f9ddb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cotton Plugged IVF Pasteur Pipets |
Version Model Number | PP-5.75-1000PL |
Company DUNS | 801895244 |
Company Name | Coopersurgical, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20888937014062 [Package] Contains: 50888937014063 Package: [20 Units] In Commercial Distribution |
GS1 | 50888937014063 [Primary] |
MQK | Labware, Assisted Reproduction |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-23 |
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