Primary Device ID | 03600040995310 |
NIH Device Record Key | 1bb3ea1b-9557-46fe-8f99-2bc70fecf5ab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ReTrace |
Version Model Number | ASXL12 |
Catalog Number | ASXL12 |
Company DUNS | 305524696 |
Company Name | Coloplast A/S |
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)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com | |
Phone | +1(800)258-3476 |
urology@coloplast.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03600040995303 [Primary] |
GS1 | 03600040995310 [Package] Contains: 03600040995303 Package: Retail Box [1 Units] In Commercial Distribution |
GS1 | 03600040995327 [Package] Package: Shipper Box [24 Units] In Commercial Distribution |
FED | endoscopic access overtube, gastroenterology-urology |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-28 |
Device Publish Date | 2024-11-20 |
03600040995389 | AXXL12 |
03600040995341 | AXXL10 |
03600040995310 | ASXL12 |
03600040995280 | ASXL10 |
03600040995259 | ALXL12 |
03600040995235 | ALXL10 |
03600040995198 | ACXL12 |
03600040995167 | ACXL10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RETRACE 97605031 not registered Live/Pending |
Graf Research Corporation 2022-09-23 |
RETRACE 90290340 not registered Live/Pending |
Impressive Sales Inc. 2020-10-30 |
RETRACE 88515345 not registered Live/Pending |
Code Walker, LLC 2019-07-15 |
RETRACE 88514229 not registered Live/Pending |
Columbia Insurance Company 2019-07-15 |
RETRACE 85181617 4231605 Dead/Cancelled |
Celestron Acquisition, LLC 2010-11-19 |
RETRACE 79333352 not registered Live/Pending |
Retrace Group Limited 2021-05-18 |
RETRACE 79081987 3924912 Live/Registered |
Coloplast A/S 2010-03-10 |
RETRACE 74522331 1986096 Dead/Cancelled |
DeRoyal Industries, Inc. 1994-05-04 |