| Primary Device ID | 20884527014948 |
| NIH Device Record Key | 1a747476-c7a4-4e69-a779-ec63fa038a8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Xeroform |
| Version Model Number | 8884433500 |
| Catalog Number | 8884433500 |
| Company DUNS | 080935429 |
| Company Name | Cardinal Health, Inc. |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Length | 4 Inch |
| Width | 4 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884527014941 [Primary] |
| GS1 | 20884527014948 [Package] Contains: 10884527014941 Package: PACK_OR_INNER_PACK [25 Units] In Commercial Distribution |
| GS1 | 30884527014945 [Package] Contains: 10884527014941 Package: CASE [150 Units] In Commercial Distribution |
| FRO | Dressing, wound, drug |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-06-17 |
| Device Publish Date | 2018-06-30 |
| 20884527014955 | Occlusive Gauze Strip,3% Bismuth Tribromophenate in Petrolatum Blend |
| 10884527014927 | Occlusive Gauze Strip,3% Bismuth Tribromophenate in Petrolatum Blend |
| 20884527014948 | Occlusive Gauze Patch,3% Bismuth Tribromophenate in Petrolatum Blend |
| 30884527014938 | Occlusive Gauze Patch,3% Bismuth Tribromophenate in Petrolatum Blend |
| 20884527014917 | Occlusive Gauze Roll,3% Bismuth Tribromophenate in Petrolatum Blend |
| 20884527014900 | Occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Petrolatum Blend |
| 20884527014894 | Occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Petrolatum Blend |
| 30884527014990 | Non-occlusive Roll,3% Bismuth Tribromophenate in Oil Emulsion |
| 40884527014980 | Non-occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Oil Emulsion |
| 30884527014976 | Non-occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Oil Emulsion |
| 30884527014969 | Non-occlusive Patch,3% Bismuth Tribromophenate in Oil Emulsion |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() XEROFORM 97598702 not registered Live/Pending |
Roosin Medical Co.,ltd. 2022-09-20 |
![]() XEROFORM 73743750 not registered Dead/Abandoned |
ABSORBENT COTTON COMPANY 1988-08-02 |