DynaSorb Super Absorbent Dressing, Self-Adherent
- Primary DI
- 00616784308920
- Brand
- DynaSorb Super Absorbent Dressing, Self-Adherent
- Company
- DYNAREX CORPORATION
- Model
- 3089
- Device description
- DynaSorb Super Absorbent Dressing, Self-Adherent, 4"x4"
- Published
- 2021-06-21
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- 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 |
|---|
| 00616784308920 | Package | GS1 | 10 | In Commercial Distribution |
| 00616784308937 | Package | GS1 | 12 | In Commercial Distribution |
| 00616784308913 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00616784308920 | 00616784308920 | 616784308920 | 0616784308920 |
| 00616784308937 | 00616784308937 | 616784308937 | 0616784308937 |
| 00616784308913 | 00616784308913 | 616784308913 | 0616784308913 |
GMDN Terms
| Term | Definition |
|---|
| Exudate-absorbent dressing, non-gel, non-antimicrobial | A wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused. |
Regulatory Flags
- DUNS number
- 008124539
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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