Primary Device ID | 20888937010927 |
NIH Device Record Key | 7eaac0c5-262e-407d-8c04-33e786cb64ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Potocky Needle® |
Version Model Number | 6066 |
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 | 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 | 20888937010927 [Primary] |
HEE | Set, Anesthesia, Paracervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-28 |
20888937010934 | Potocky Needle® For Intra Cervical Block |
20888937010927 | Potocky Needle® For Intra Cervical Block |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
POTOCKY NEEDLE 74152197 1763649 Live/Registered |
CooperSurgical, Inc. 1991-03-28 |