Primary Device ID | 10653160386360 |
NIH Device Record Key | 5a8d191a-e14f-4fad-8ec7-14234a2e7408 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Centurion |
Version Model Number | FCS200ZTKT |
Catalog Number | FCS200ZTKT |
Company DUNS | 017246562 |
Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
Device Count | 1 |
DM Exempt | true |
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 | 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(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM | |
Phone | +1(517)546-5400 |
CUSTOMERSERVICE@CENTURIONMP.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10653160386360 [Package] Contains: 20653160386367 Package: CASE [50 Units] In Commercial Distribution |
GS1 | 20653160386367 [Primary] |
EYJ | HOLDER, URETERAL CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-24 |
Device Publish Date | 2025-02-14 |