FDA UDI
In Commercial Distribution
🇺🇸 United States
Curity
DI: 20192253023876
·
Model: FH-PADORG
·
Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
14
Basic Information
- Brand Name
- Curity
- Primary DI
- 20192253023876
- Version / Model
- FH-PADORG
- Catalog Number
- FH-PADORG
- Company Name
- Cardinal Health 200, LLC
- Labeler DUNS
- 961027315
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 14
- Record Status
- Published
- Publish Date
- 2020-07-21
- Public Version
- 1
- Public Version Date
- 2020-07-29
- Public Version Status
- New
- Public Device Record Key
- 36b6047c-3c28-42a6-83f1-ceb57b548927
Device Description
Maxi Pad Curity 6.26 x 12.2 in. (15.9 x 31.0 cm) Ultra thin Unscented Overnight with wings Materials of fabrication: Topsheet (skin contact): is bicomponent Polyethylene / Polypropylene Acquistion Distribution Layer: is a nonwoven hightloft layer made of polyester Absorbent Core: cellulose fibers with a super absorbent polymer Backsheet (external layer): is a nonwoven made of polyethylene Includes a release silicone paper and polyolefin adhesives in the seams and joints
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
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| HHD | Pad, menstrual, unscented | Obstetrics/Gynecology | 884.5435 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 40545 | Menstrual pad, unscented | A non-deodorized, feminine hygiene product (a pad) that is held in place externally to absorb menstrual or other vaginal discharge. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 50192253023877 | GS1 | CASE | 12 | In Commercial Distribution | |
| Primary | 20192253023876 | GS1 | ||||
| Unit of Use | 10192253023879 | GS1 |