ReTrace ASXL12

GUDID 03600040995310

Coloplast A/S

Ureteral introduction sheath
Primary Device ID03600040995310
NIH Device Record Key1bb3ea1b-9557-46fe-8f99-2bc70fecf5ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameReTrace
Version Model NumberASXL12
Catalog NumberASXL12
Company DUNS305524696
Company NameColoplast A/S
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com
Phone+1(800)258-3476
Emailurology@coloplast.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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, SpecifyBetween 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 Identifiers

Device Issuing AgencyDevice ID
GS103600040995303 [Primary]
GS103600040995310 [Package]
Contains: 03600040995303
Package: Retail Box [1 Units]
In Commercial Distribution
GS103600040995327 [Package]
Package: Shipper Box [24 Units]
In Commercial Distribution

FDA Product Code

FEDendoscopic access overtube, gastroenterology-urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-28
Device Publish Date2024-11-20

On-Brand Devices [ReTrace]

03600040995389AXXL12
03600040995341AXXL10
03600040995310ASXL12
03600040995280ASXL10
03600040995259ALXL12
03600040995235ALXL10
03600040995198ACXL12
03600040995167ACXL10

Trademark Results [ReTrace]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RETRACE
RETRACE
97605031 not registered Live/Pending
Graf Research Corporation
2022-09-23
RETRACE
RETRACE
90290340 not registered Live/Pending
Impressive Sales Inc.
2020-10-30
RETRACE
RETRACE
88515345 not registered Live/Pending
Code Walker, LLC
2019-07-15
RETRACE
RETRACE
88514229 not registered Live/Pending
Columbia Insurance Company
2019-07-15
RETRACE
RETRACE
85181617 4231605 Dead/Cancelled
Celestron Acquisition, LLC
2010-11-19
RETRACE
RETRACE
79333352 not registered Live/Pending
Retrace Group Limited
2021-05-18
RETRACE
RETRACE
79081987 3924912 Live/Registered
Coloplast A/S
2010-03-10
RETRACE
RETRACE
74522331 1986096 Dead/Cancelled
DeRoyal Industries, Inc.
1994-05-04

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