Primary Device ID | 00888937019834 |
NIH Device Record Key | 3c2ce0e2-f80e-4693-b4b6-ee1e7f2b3d55 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wallach Accu-Shield |
Version Model Number | 900108 |
Company DUNS | 801895244 |
Company Name | Coopersurgical, Inc. |
Device Count | 1 |
DM Exempt | false |
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 | false |
Lot Batch | true |
Serial Number | false |
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 | 00888937019834 [Primary] |
HDQ | Dilator, Cervical, Fixed Size |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-25 |
Device Publish Date | 2022-11-17 |
00888937026870 - Mara Console | 2024-03-21 Mara Console- Endometrial Ablation |
00888937023817 - K-Systems | 2024-02-27 L126 IVF, Standard Heat Right |
00888937023824 - K-Systems | 2024-02-27 L126 IVF, Standard Heat Right |
00888937023831 - K-Systems | 2024-02-27 L126 IVF, RI Witness Right |
00888937023848 - K-Systems | 2024-02-27 L126 IVF, RI Witness Right |
00888937023855 - K-Systems | 2024-02-27 L126 IVF, Standard Heat Right, Monitor |
00888937023862 - K-Systems | 2024-02-27 L126 IVF, Standard Heat Right, Monitor |
00888937023879 - K-Systems | 2024-02-27 L126 IVF, RI Witness Right, Monitor |