MICROFLEX
- Primary DI
- 00769799288098
- Brand
- MICROFLEX
- Company
- Ansell Healthcare Product
- Model
- NEC-288-XL
- Catalog number
- NEC-288-XL
- Device description
- MICROFLEX NEC-288 NEOPRO EC SIZE XL (9.5-10.0), Neoprene Powder-Free Examination Glove
- Published
- 2022-03-14
- 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
Related Records
Contact Domains
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 |
|---|---|---|---|---|
| 00769799288098 | Package | GS1 | 10 | In Commercial Distribution |
| 00769799288197 | Primary | GS1 | 0 | |
| 00071483003611 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00769799288098 | 00769799288098 | 769799288098 | 0769799288098 |
| 00769799288197 | 00769799288197 | 769799288197 | 0769799288197 |
| 00071483003611 | 00071483003611 | 071483003611 | 0071483003611 |
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. |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| 775-746-6600 | jacob.ramirez@ansell.com |
Regulatory Flags
- DUNS number
- 111267330
- Device count
- 50
- 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
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company
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|---|---|---|---|---|
| 20076490793160 | MICROFLEX | XC-310CP-XS | XC-310CP-XS | 2025-08-05 |
| 20076490793177 | MICROFLEX | XC-310CP-S | XC-310CP-S | 2025-08-05 |
| 20076490793184 | MICROFLEX | XC-310CP-M | XC-310CP-M | 2025-08-05 |
| 20076490793191 | MICROFLEX | XC-310CP-L | XC-310CP-L | 2025-08-05 |
| 20076490793207 | MICROFLEX | XC-310CP-XL | XC-310CP-XL | 2025-08-05 |
| 10076490456518 | TOUCHNTUFF | 69318060 | 69318060 | 2025-07-30 |
| 20076490001463 | TOUCHNTUFF | 69318070 | 69318070 | 2025-07-30 |
| 20076490001470 | TOUCHNTUFF | 69318080 | 69318080 | 2025-07-30 |
| 20076490001487 | TOUCHNTUFF | 69318090 | 69318090 | 2025-07-30 |
| 20076490001494 | TOUCHNTUFF | 69318100 | 69318100 | 2025-07-30 |
| 20076490721248 | KIMTECH | 62760 | 62760 | 2025-07-21 |
| 20076490727141 | KIMTECH | 62761 | 62761 | 2025-07-21 |
| 20076490729312 | KIMTECH | 62764 | 62764 | 2025-07-21 |
| 20076490736495 | KIMTECH | 62763 | 62763 | 2025-07-21 |
| 20076490750088 | KIMTECH | 62762 | 62762 | 2025-07-21 |
| 20076490724171 | KIMTECH | 50602 | 50602 | 2025-07-03 |
| 20076490730592 | KIMTECH | 50709 | 50709 | 2025-07-03 |
| 20076490748658 | KIMTECH | 55090 | 55090 | 2025-07-03 |
| 20076490750262 | KIMTECH | 50604 | 50604 | 2025-07-03 |
| 20076490754888 | KIMTECH | 50706 | 50706 | 2025-07-03 |
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