DynaSorb Super Absorbent Dressing, Non-Adherent
- Primary DI
- 00616784308722
- Brand
- DynaSorb Super Absorbent Dressing, Non-Adherent
- Company
- DYNAREX CORPORATION
- Model
- 3087
- Device description
- DynaSorb Super Absorbent Dressing, Non-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 |
|---|
| 00616784308722 | Package | GS1 | 10 | In Commercial Distribution |
| 00616784308739 | Package | GS1 | 12 | In Commercial Distribution |
| 00616784308715 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00616784308722 | 00616784308722 | 616784308722 | 0616784308722 |
| 00616784308739 | 00616784308739 | 616784308739 | 0616784308739 |
| 00616784308715 | 00616784308715 | 616784308715 | 0616784308715 |
GMDN Terms
| Term | Definition |
|---|
| Wound-nonadherent dressing, absorbent, non-antimicrobial | A wound covering typically in the form of a multi-layered pad having a material or substance on its skin-contact surface (e.g., silicone gel), or designed to be soaked in saline prior to application, to prevent adherence to the wound bed thereby decreasing wound trauma potential; it does not contain an antimicrobial agent. It is typically used to absorb wound blood/exudates while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites; it is not a dedicated burn dressing. This is a single-use device. |
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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