FDA UDI
In Commercial Distribution
🇺🇸 United States
Kendall
DI: 00884521166816
·
Model: 55523BG
·
Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- Kendall
- Primary DI
- 00884521166816
- Version / Model
- 55523BG
- Catalog Number
- 55523BG
- Company Name
- Cardinal Health, Inc.
- Labeler DUNS
- 080935429
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-06-30
- Public Version
- 5
- Public Version Date
- 2024-02-29
- Public Version Status
- Update
- Public Device Record Key
- 5003adf4-06d2-4c3d-8af1-662b51b73ff6
- Distribution End Date
- 2025-12-31
Device Description
Foam Border Gentle Adhesion,1 Inch x 1-3/4 Inch (2.5 cm x 4.4 cm) Pad
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
- 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 |
|---|---|---|---|---|
| NAD | Dressing, wound, occlusive | General, Plastic Surgery | 878.4020 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 43186 | Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial | A wound covering, typically made of a hydrocolloid, hydrofibre, chitosan or alginate (salts and acids extracted from seaweed), intended to produce a water-absorbent gel upon contact with wound exudate; it does not contain an antimicrobial agent. The device assists in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) for minimal wound maceration, allowing wound debridement, and creating a moist wound-healing environment. The device may be in the form of a flat sheet/film, ribbon, rope, foam, liquid, paste, 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 | 00884521166830 | GS1 | PACK_OR_INNER_PACK | 10 | In Commercial Distribution | 2025-12-31 |
| Primary | 00884521166816 | GS1 | ||||
| Package | 00884521166854 | GS1 | CASE | 50 | In Commercial Distribution | 2025-12-31 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Width | 1.75 | Inch | |
| Length | 3.25 | Inch |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- ;AVOID DIRECT SUNLIGHT