Revital-Ox Resert
- Primary DI
- 00724995095017
- Brand
- Revital-Ox Resert
- Company
- STERIS CORPORATION
- Model
- 4455AW
- Catalog number
- 4455AW
- Device description
- Revital-Ox Resert High Level Disinfectant is a reusable high level disinfectant for processing semi-critical medical devices for which alternative methods of terminal processing are not suitable or available. It is for use in both manual soaking and automated endoscope processors. It must be used with Revital-Ox RESERT R60 Solution Test Strips.
- Published
- 2016-09-07
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- true
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MED | Sterilant, medical devices |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MED | Sterilant, Medical Devices | General Hospital | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 50724995095012 | Package | GS1 | 4 | In Commercial Distribution |
| 00724995095017 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 50724995095012 | 50724995095012 | ||
| 00724995095017 | 00724995095017 | 724995095017 | 0724995095017 |
GMDN Terms#
| Term | Definition |
|---|---|
| Medical device disinfection agent | A non-patient-contact substance containing a chemical agent(s) intended to destroy microorganisms or inhibit their activity (disinfectant) on medical instrumentation, equipment, and/or facility surfaces (excluding use on contact lenses). It may contain surfactants/cleaning agents or enzymes (e.g., protease, lipase), and may be intended to decalcify equipment. The medical device is intended to be exposed to the substance to achieve disinfection through bathing, wiping, and/or in combination with a disinfection device. It is available in liquid, aerosol, powder, or tablet form; it is not supplied in a dedicated wipe, cap, or other contact-application carrier. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Total Volume | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep in original container |
| Storage Environment Humidity | 0 | 0 | |
| Storage Environment Temperature | 0 | 0 |
Contacts#
| Phone | |
|---|---|
| +1(800)548-4873 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 139424188
- Device count
- 1
- 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
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
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|---|---|---|---|---|
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| 10724995023833 | VERIFY | Dual Species | S306 | 2016-09-09 |
| 10724995032798 | DART | NB113 | NB113 | 2016-09-09 |
| 10724995154735 | VERIFY SIXCESS | PCC072 | PCC072 | 2019-04-19 |
| 10724995154742 | VERIFY SIXCESS | PCC073 | PCC073 | 2019-04-19 |
| 00724995000783 | Revital-Ox Resert | 4455N9 | 4455N9 | 2016-09-07 |
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