Primary Device ID | 00888937010367 |
NIH Device Record Key | 800c8b16-7b62-4c9c-b658-f338991ee4c1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medi Choice |
Version Model Number | MC150A-SD5 |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
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 | 00888937010367 [Primary] |
HEP | Monitor, Blood-Flow, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-07-20 |
00888937018240 - Lone Star® IRI Delivery | 2024-07-01 Lone Star® IRI Delivery Tube Replacement |
00888937026597 - LEEP PRECISION™ Smoke Evacuator | 2024-06-25 LEEP PRECISION™ Smoke Evacuator (230 VAC) |
60888937027176 - ERPeak | 2024-04-18 IVD Sample kit |
60888937027183 - ERPeak | 2024-04-18 IVD Sample kit |
60888937027190 - ERPeak | 2024-04-18 IVD Sample kit |
60888937027206 - ERPeak | 2024-04-18 IVD Sample kit |
00888937026870 - Mara Console | 2024-03-21 Mara Console- Endometrial Ablation |
00888937023817 - K-Systems | 2024-02-27 L126 IVF, Standard Heat Right |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDI CHOICE 74717337 not registered Dead/Abandoned |
Reichert, Cari McBroom 1995-08-18 |