Conveen Security+
- Primary DI
- 05708932539302
- Brand
- Conveen Security+
- Company
- Coloplast A/S
- Model
- 21029
- Catalog number
- 21029
- Device description
- Conveen Security+. Urine collection bag. Leg bag. Sterile. Inlet tube: 2.4 inch (6 cm). Incl. 10 x strap set (sterile). Volume: 17 oz (500 ml).
- Published
- 2022-03-11
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Rx
- false
- OTC
- true
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| FAQ | BAG, URINE COLLECTION, LEG, FOR EXTERNAL USE, STERILE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FAQ | Bag, Urine Collection, Leg, For External Use, Sterile | Gastroenterology, Urology | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05708932539302 | Package | GS1 | 10 | In Commercial Distribution |
| 05708932539319 | Package | GS1 | 6 | In Commercial Distribution |
| 05708932539296 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05708932539302 | 05708932539302 | 5708932539302 |
| 05708932539319 | 05708932539319 | 5708932539319 |
| 05708932539296 | 05708932539296 | 5708932539296 |
GMDN Terms#
| Term | Definition |
|---|---|
| Wearable adult urine collection bag, open-ended | A flexible plastic pouch designed to connect to a urinary catheter or a urinary condom catheter and to be strapped to or worn on the leg of an adult/adolescent patient to collect discharged urine; it is designed with an opening for urine drainage. Also known as a leg bag, it is worn on the body to facilitate patient mobility. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 6 | Centimeter |
| Total Volume | 17 | Fluid Ounce |
| Total Volume | 500 | Milliliter |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Do not use if package is damaged and consult IFU. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 305524696
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- 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
- true
- Sterilization required before use
- false
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