Primary Device ID | 10801741097833 |
NIH Device Record Key | e3c17cc4-4d57-4585-b985-87fb9d8901f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Magic3 Go™ Intermittent Urinary Catheter |
Version Model Number | 51808 |
Catalog Number | 51808 |
Company DUNS | 016898496 |
Company Name | C. R. Bard, 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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com |
Catheter Gauge | 8 French |
Catheter Gauge | 8 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741097836 [Primary] |
GS1 | 10801741097833 [Package] Contains: 00801741097836 Package: CA [30 Units] In Commercial Distribution |
EZD | CATHETER, STRAIGHT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-10-28 |
10801741098083 | Magic3 Go® Intermittent Urinary Catheter |
10801741097932 | Magic3 Go® Intermittent Urinary Catheter |
10801741097895 | Magic3 Go® Intermittent Urinary Catheter |
10801741097871 | Magic3 Go® Intermittent Urinary Catheter |
10801741097857 | Magic3 Go® Intermittent Urinary Catheter |
10801741097833 | Magic3 Go™ Intermittent Urinary Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAGIC3 GO 86350788 5003908 Live/Registered |
Rochester Medical Corporation 2014-07-29 |