Primary Device ID | 10753567101204 |
NIH Device Record Key | 54236703-c9b2-4608-b0ca-0db21dc72eb7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UC Strip™ |
Version Model Number | UC-20 |
Catalog Number | DERMA-UC20 |
Company DUNS | 200564891 |
Company Name | Derma Sciences Canada Inc |
Device Count | 20 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00753567101207 [Unit of Use] |
GS1 | 10753567101204 [Primary] |
FPX | Strip, adhesive, closure, skin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-11-07 |
Device Publish Date | 2019-03-08 |
30381780471312 - XEROFORM PETROLATUM | 2022-11-07 Petrolatum Dressing. Fine Mesh Gauze Impregnated with 3% Bismuth Tribromophenate in a Petrolatum Blend. |
30381780471329 - XEROFORM PETROLATUM | 2022-11-07 Petrolatum Dressing. Fine Mesh Gauze Impregnated with 3% Bismuth Tribromophenate in a Petrolatum Blend. |
30381780471336 - XEROFORM PETROLATUM | 2022-11-07 Petrolatum Dressing. Fine Mesh Gauze Impregnated with 3% Bismuth Tribromophenate in a Petrolatum Blend. |
30381780471343 - XEROFORM PETROLATUM | 2022-11-07 Xeroform Petrolatum Impregnated Gauze |
30381780486828 - MediHoney® | 2022-11-07 Dressing with Active Leptospermum Honey |
30381780486934 - MEDIHONEY® Paste | 2022-11-07 Dressing with Active LeptospermumHoney |
30381780486958 - MEDIHONEY® HCS | 2022-11-07 (NON-ADHESIVE FENESTRATED) HYDROGEL COLLOIDAL SHEET with LEPTOSPERMUM HONEY |
30381780486965 - MEDIHONEY® HCS | 2022-11-07 (ADHESIVE) HYDROGEL COLLOIDAL SHEET with LEPTOSPERMUM HONEY |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UC STRIP 75112711 2077308 Dead/Cancelled |
Genetic Laboratories Wound Care Inc. 1996-06-03 |