FDA UDI
In Commercial Distribution
🇺🇸 United States
Protect U Guard Hydrocolloid Sterile Dressing
DI: B086191031
·
Model: P19103
·
PROTECT U GUARD, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10
Basic Information
- Brand Name
- Protect U Guard Hydrocolloid Sterile Dressing
- Primary DI
- B086191031
- Version / Model
- P19103
- Company Name
- PROTECT U GUARD, LLC
- Labeler DUNS
- 080070945
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 10
- Record Status
- Published
- Publish Date
- 2020-08-21
- Public Version
- 1
- Public Version Date
- 2020-08-31
- Public Version Status
- New
- Public Device Record Key
- 7deeb718-d843-4d6b-8bd8-fda46257c073
Device Description
Protect U Guard Hydrocolloid Sterile Dressing Oval/Heel 4x7cm
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- Yes
- 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
- No
- 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 |
|---|---|---|---|---|
| 48124 | Exudate-absorbent dressing, non-gel, antimicrobial | A wound covering intended to absorb exudates and blood from a wound (e.g., ulcers, burns, surgical wounds, lacerations, abrasions, and/or percutaneous device wounds), and that contains an antimicrobial agent [e.g., silver (Ag), chlorhexidine gluconate (CHG)]. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudate. It is intended to create a moist wound-healing environment and/or protect wounds from external contamination by microorganisms from the periwound skin. 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. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | B086291032 | HIBCC | CARTON | 800 | In Commercial Distribution | |
| Primary | B086191031 | HIBCC | ||||
| Unit of Use | B086091030 | HIBCC |
Customer Contacts
- Phone
- 8138150530
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Width | 4 | Centimeter | |
| Length | 7 | Centimeter |