CARDINAL HEALTH
- Primary DI
- 50885380134812
- Brand
- CARDINAL HEALTH
- Company
- CARDINAL HEALTH 200, LLC
- Model
- 8844XL
- Catalog number
- 8844XL
- Device description
- Latex Exam Gloves
- Published
- 2019-01-30
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- true
- Sterile
- false
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| LYY | Latex patient examination glove |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LYY | Latex Patient Examination Glove | General Hospital | 1 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K093375 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 50885380134812 | Package | GS1 | 10 | In Commercial Distribution |
| 00885380134817 | Primary | GS1 | 0 | |
| 10885380134814 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 50885380134812 | 50885380134812 | ||
| 00885380134817 | 00885380134817 | 885380134817 | 0885380134817 |
| 10885380134814 | 10885380134814 |
GMDN Terms#
| Term | Definition |
|---|---|
| Hevea-latex examination/treatment glove, non-powdered, non-sterile | A non-sterile device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with talcum powder and it does not have antimicrobial features. The device is used mainly as a two-way barrier to protect both the patient and the staff against various contamination. It will have appropriate characteristics regarding tactility/comfort of use, and should provide appropriate physical properties (e.g., strength, elasticity), and uniformity of dimensions. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 112164780
- Device count
- 100
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- true
- No natural rubber latex
- false
- Sterilization required before use
- false
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