Primary Device ID | 05701780360029 |
NIH Device Record Key | e972980d-bdd7-4c5e-a70f-61433ecf2a71 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SenSura Mio |
Version Model Number | 19794 |
Catalog Number | 19794 |
Company DUNS | 305524696 |
Company Name | Coloplast A/S |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com | |
Phone | +1(800)533-0464 |
healthcarecs@coloplast.com |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 50 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05701780359979 [Primary] |
GS1 | 05701780360029 [Package] Contains: 05701780359979 Package: Shipper Box [16 Units] In Commercial Distribution |
GS1 | 05701780360036 [Unit of Use] |
EXB | Collector, ostomy |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-05 |
Device Publish Date | 2025-04-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SENSURA MIO 79139969 4590839 Live/Registered |
Coloplast A/S 2013-09-16 |