CARDINAL HEALTH
- Primary DI
- 00888499000837
- Brand
- CARDINAL HEALTH
- Company
- Cardinal Health 200, LLC
- Model
- COMP23
- Catalog number
- COMP23
- Device description
- Composite Dressing 2 x 3 in. Superficial and non-infected wounds: -Post-operative wounds -Skin grafts and donor sites -Lacerations and abrasions -Minor burns and scalds
- Published
- 2019-05-31
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- true
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| NAC | Dressing, wound, hydrophilic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| NAC | Dressing, Wound, Hydrophilic | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888499000837 | Package | GS1 | 1 | In Commercial Distribution |
| 10888499000834 | Package | GS1 | 20 | In Commercial Distribution |
| 10885380064906 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888499000837 | 00888499000837 | 888499000837 | 0888499000837 |
| 10888499000834 | 10888499000834 | ||
| 10885380064906 | 10885380064906 |
GMDN Terms#
| Term | Definition |
|---|---|
| Exudate-absorbent dressing, hydrophilic-gel, antimicrobial | A wound covering, typically made of a hydrocolloid, hydrofibre, chitosan or alginate (salts and acids extracted from seaweed), intended to produce a water-absorbent gel upon contact with wound exudate, and that contains an antimicrobial agent [e.g., silver (Ag), honey]. It assists in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) for minimal wound maceration, allowing wound debridement, and creating a moist wound-healing environment while reducing microbial colonization within the dressing. The device may be in the form of a flat sheet/film, ribbon, rope, foam, liquid, or powder. After application, this device cannot be reused. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 Degrees Celsius | 35 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 961027315
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 10198956388239 | CARDINAL HEALTH | SOT53CYPOF | SOT53CYPOF | 2026-09-25 |
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| 10198956466838 | CARDINAL HEALTH | SNE35LSFSG | SNE35LSFSG | 2026-09-25 |
| 10198956484382 | CARDINAL HEALTH | ANE306276A | ANE306276A | 2026-09-25 |
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