Primary Device ID | 20884527021205 |
NIH Device Record Key | 51445ab2-1704-451f-b0d9-4a965d22e50e |
Commercial Distribution Discontinuation | 2025-12-31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dermacea |
Version Model Number | 441124 |
Catalog Number | 441124 |
Company DUNS | 080935429 |
Company Name | Cardinal Health, Inc. |
Device Count | 12 |
DM Exempt | false |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Device Size Text, specify | 0 |
Width | 2 Inch |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Special Storage Condition, Specify | Between 0 and 0 *This side up; |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884527021208 [Primary] |
GS1 | 20884527021205 [Package] Contains: 10884527021208 Package: CASE [96 Units] Discontinued: 2025-12-31 In Commercial Distribution |
GS1 | 30884527021202 [Unit of Use] |
NAB | Gauze / sponge,nonresorbable for external use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-10-30 |
Device Publish Date | 2018-06-29 |
00884521067182 | Abdominal Pad |
00884527017266 | Abdominal Pad |
00884521067168 | Abdominal Pad |
00884527017242 | Abdominal Pad |
00884521060596 | Abdominal Pad |
00884527017129 | Abdominal Pad |
20884527021021 | Stretch Bandage Roll |
40884521143808 | Stretch Bandage Roll |
10884521065284 | Dressing in Strippable Envelope |
10884521065277 | Dressing in Strippable Envelope |
10884521066045 | Gauze Sponges,8 Ply |
50885380173521 | True content to be populated as part of rebranding |
50885380174597 | True content to be populated as part of rebranding |
30885380174586 | True content to be populated as part of rebranding |
30885380174579 | True content to be populated as part of rebranding |
30885380174562 | True content to be populated as part of rebranding |
50885380173668 | True content to be populated as part of rebranding |
50885380173651 | True content to be populated as part of rebranding |
50885380173644 | True content to be populated as part of rebranding |
20884521065298 | Dressing in Strippable Envelope |
10884521143791 | True content to be populated as part of rebranding |
20884527015723 | Stretch Bandage |
20884527015716 | Stretch Bandage |
20884527015709 | Stretch Bandage |
30884527015690 | Stretch Bandage |
30884527015683 | Stretch Bandage |
30884527015676 | Stretch Bandage |
20884527015662 | Stretch Bandage |
20884527021267 | X-Ray Sponges,24 Ply |
20884527021250 | X-Ray Sponges,24 Ply |
20884527021243 | X-Ray Sponges,12 Ply |
20884527021236 | X-Ray Sponges,16 Ply |
20884527021182 | Gauze Roll,3 Ply |
20884527021175 | Gauze Roll,3 Ply |
20884527021090 | USP Type VII Gauze,12 Ply |
20884527021083 | X-Ray Sponges,16 Ply |
20884527021076 | X-Ray Sponges,16 Ply |
20884527021069 | X-Ray Sponges,12 Ply |
20884527020994 | Non-woven Sponges,6 Ply |
20884527020949 | Gauze Roll,3 Ply |
20884527020932 | True content to be populated as part of rebranding |
20884527020918 | X-Ray Sponges,16 Ply |
20884521174877 | Super Sponges,Medium |
20884521148151 | USP Type VII Gauze,8 Ply |
20884521128696 | USP Type VII Gauze,16 Ply |
20884521084305 | USP Type VII Gauze,16 Ply |
20884521084299 | USP Type VII Gauze,12 Ply |
20884521084282 | USP Type VII Gauze,12 Ply |
20884521084275 | USP Type VII Gauze,12 Ply |
20884521084268 | USP Type VII Gauze,8 Ply |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DERMACEA 78700731 not registered Dead/Abandoned |
NutraCea, Inc. 2005-08-25 |
DERMACEA 78399227 2999232 Live/Registered |
CARDINAL HEALTH 529, LLC 2004-04-09 |
DERMACEA 74441406 1920675 Dead/Cancelled |
SHERWOOD MEDICAL COMPANY 1993-09-29 |
DERMACEA 72365270 0905261 Dead/Expired |
PETTIBONE LABORATORIES, INC. 1970-07-15 |