Criterion CR4G Chlor Glove
- Primary DI
- 20304040102385
- Brand
- Criterion CR4G Chlor Glove
- Company
- HENRY SCHEIN, INC.
- Model
- 1127306
- Catalog number
- 1127306
- Device description
- Criterion CR4G Chlor Glove X-Small
- Published
- 2020-01-08
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| LZA | Polymer patient examination glove |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LZA | Polymer Patient Examination Glove | General Hospital | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20304040102385 | Package | GS1 | 10 | In Commercial Distribution |
| 10304040102388 | Primary | GS1 | 0 | |
| 00304040102381 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20304040102385 | 20304040102385 | ||
| 10304040102388 | 10304040102388 | ||
| 00304040102381 | 00304040102381 | 304040102381 | 0304040102381 |
GMDN Terms
| Term | Definition |
|---|---|
| Polychloroprene examination/treatment glove, non-powdered | A non-sterile device made of polychloroprene (neoprene) 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 patient/staff against contaminants and risk of allergy to latex. 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. |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | FALSE |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 012430880
- Device count
- 100
- DM exempt
- true
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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