Primary Device ID | 60888937016576 |
NIH Device Record Key | 4426c2b3-311c-4d86-8677-cae210b778bf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HSG Procedure Tray, 5Fr |
Version Model Number | 19612 |
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 | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 60888937016576 [Primary] |
LKF | Cannula, Manipulator/Injector, Uterine |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-14 |
Device Publish Date | 2018-08-14 |
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