Primary Device ID | 00827002249745 |
NIH Device Record Key | 164aedeb-38e3-4dd9-81d1-a2dc55cfc6f8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lehman |
Version Model Number | G24974 |
Catalog Number | SOM-18-L-LEHMAN-NG |
Company DUNS | 079720472 |
Company Name | COOK INCORPORATED |
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 |
Phone | +1(812)330-5494 |
sharedservices@cookmedical.com |
Special Storage Condition, Specify | Between 0 and 0 *Store in dark, dry, cool place. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00827002249745 [Primary] |
FFX | SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-09-24 |
00827002249745 | Lehman Manometry Catheter |
00827002249721 | Lehman Manometry Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LEHMAN 98016489 not registered Live/Pending |
PEABODY, MORGAN & CO., INC. 2023-05-26 |
LEHMAN 73597614 not registered Dead/Abandoned |
LEHMAN MANUFACTURING CO., INC. 1986-05-08 |
LEHMAN 72220585 0863317 Live/Registered |
UNITED STATES CATHETER & INSTRUMENT CORPORATION 1965-06-07 |