Banicide Plus Sterilizing and Disinfecting Solution
- Primary DI
- 00310866000008
- Brand
- Banicide Plus Sterilizing and Disinfecting Solution
- Company
- PASCAL COMPANY, INC.
- Model
- 15200
- Catalog number
- 15200
- Device description
- Reusable 3.4% Glutaraldehyde Sterilizing & Disinfecting Solution; 1 gallonSterilization, high level disinfection and cleaning/decontamination solution.
- Published
- 2019-01-29
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
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 |
|---|---|---|---|---|
| 10310866000005 | Package | GS1 | 4 | In Commercial Distribution |
| 20310866000002 | Package | GS1 | 144 | In Commercial Distribution |
| 00310866000008 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10310866000005 | 10310866000005 | ||
| 20310866000002 | 20310866000002 | ||
| 00310866000008 | 00310866000008 | 310866000008 | 0310866000008 |
GMDN Terms#
| Term | Definition |
|---|---|
| Glutaraldehyde device sterilant | A liquid substance that includes glutaraldehyde as its primary agent intended to completely destroy or eliminate (sterilize) all harmful microorganisms on a medical device (e.g., surgical or dental instrument); it may also be intended for use as a high-level disinfectant. The medical device is typically bathed by the substance for a specified period of time in order to achieve high-level disinfection or sterilization. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Handling Environment Temperature | 59 Degrees Fahrenheit | 86 Degrees Fahrenheit |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| 8004268051 | pascaldental@pascaldental.com |
Regulatory Flags#
- DUNS number
- 009260217
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
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| 00310866002606 | KOIS KR-2 PACKER | 26226 | 2024-06-04 | |
| 00310866002613 | KOIS KR-3 PACKER | 26227 | 2024-06-04 | |
| 00310866002620 | KOIS KR-4 PACKER | 26228 | 2024-06-04 | |
| 00310866002637 | KOIS KR-5 PACKER | 26229 | 2024-06-04 | |
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| 00310866002668 | Fluorilaq Mint (10mL) Tube | 10406 | 2024-03-28 | |
| 00310866002408 | Racord Plus Retraction Cord 7/00 | 07797 | 07797 | 2021-11-22 |
| 00310866002415 | Racord Plus Retraction Cord 8/0 | 07800 | 07800 | 2021-11-22 |
| 00310866002422 | Racord Plus Retraction Cord 9/1 | 07810 | 07810 | 2021-11-22 |
| 00310866002439 | Racord Plus Retraction Cord 10/2 | 07820 | 07820 | 2021-11-22 |
| 00310866000800 | Retrax Pellets | 12400 | 12400 | 2019-01-31 |
| 00310866000275 | KnitTrax Plain Retraction Cord 000 | 07569 | 07569 | 2019-01-29 |
| 00310866000282 | KnitTrax Plain Retraction Cord 00 | 07570 | 07570 | 2019-01-29 |
| 00310866000299 | KnitTrax Plain Retraction Cord 0 | 07575 | 07575 | 2019-01-29 |
| 00310866000305 | KnitTrax Plain Retraction Cord 1 | 07580 | 07580 | 2019-01-29 |
| 00310866000312 | KnitTrax Plain Retraction Cord 2 | 07585 | 07585 | 2019-01-29 |
| 00310866000329 | SilTrax AS Retraction Cord 7/00 | 07097 | 07097 | 2019-01-24 |
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