DynaGinate AG Silver Calcium Alginate
- Primary DI
- 00616784303215
- Brand
- DynaGinate AG Silver Calcium Alginate
- Company
- DYNAREX CORPORATION
- Model
- 3032
- Device description
- DynaGinate AG Silver Calcium Alginate, 4" x 8" (10cm x 20cm), High Absorbency, For Wound Stages 3,4
- Published
- 2022-04-25
- 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
Related Records
Product Codes
| Code | Name |
|---|---|
| FRO | Dressing, Wound, Drug |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FRO | Dressing, Wound, Drug | Unknown | U |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00616784303222 | Package | GS1 | 5 | In Commercial Distribution |
| 00616784303239 | Package | GS1 | 10 | In Commercial Distribution |
| 00616784303215 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00616784303222 | 00616784303222 | 616784303222 | 0616784303222 |
| 00616784303239 | 00616784303239 | 616784303239 | 0616784303239 |
| 00616784303215 | 00616784303215 | 616784303215 | 0616784303215 |
GMDN Terms
| Term | Definition |
|---|---|
| Cavity-wound management dressing, antimicrobial | A non-bioabsorbable material or substance designed to be inserted into a wound bed to create an appropriate environment for healing (e.g., warm, moist, absorbent), and that contains an antimicrobial agent [e.g., silver (Ag), honey]. It is typically used for the management of deep secondary-healing wounds, particularly for indications such as stage III and IV pressure ulcers, deep leg ulcers, cavity wounds, excisions, and post-op wound dehiscence. It is often designed to conform to the wound bed to support tissues and is often nonadherent to provide for patient comfort during wound management. This is a single-use device. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 008124539
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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
- false
- Sterilization required before use
- false
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