FDA UDI
In Commercial Distribution
🇺🇸 United States
Advazorb Sacral
DI: 05060031482126
·
Model: CR4501
·
BRIGHTWAKE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Advazorb Sacral
- Primary DI
- 05060031482126
- Version / Model
- CR4501
- Company Name
- BRIGHTWAKE LIMITED
- Labeler DUNS
- 226502201
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-07-27
- Public Version
- 1
- Public Version Date
- 2023-08-04
- Public Version Status
- New
- Public Device Record Key
- 417c8985-6daf-4d6c-ba6d-d5a91f8e6c87
Device Description
Absorbent foam sacral dressing with film backing, 17cm x 19cm. Advazorb Sacral is a soft, conforming, low adherent polyurethane foam wound dressing with pink polyurethane film backing and soft silicone contact layer that adheres only to normal healthy skin Advazorb Sacral has high fluid absorbency and retention characteristics. Advazorb Sacral also contributes to a pressure relieving protocol when used in conjunction with pressure relieving devices.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- Yes
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NAC | Dressing, Wound, Hydrophilic | General, Plastic Surgery | 878.4018 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46854 | 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. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 05060031482133 | GS1 | Retail | 10 | In Commercial Distribution | |
| Primary | 05060031482126 | GS1 | ||||
| Package | 05060031482140 | GS1 | Shipper | 20 | In Commercial Distribution |
Customer Contacts
- Phone
- +441623751500
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Width | 22 | Centimeter | |
| Length | 23 | Centimeter |