Kangaroo
- Primary DI
- 20884521144139
- Brand
- Kangaroo
- Company
- Cardinal Health, Inc.
- Model
- 410S
- Catalog number
- 410S
- Device description
- Purple Enteral Feeding Syringe,Tip Cap
- Published
- 2018-06-27
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| KYW | CONTAINER, LIQUID MEDICATION, GRADUATED |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KYW | Container, Liquid Medication, Graduated | General Hospital | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20884521144139 | Package | GS1 | 500 | Not in Commercial Distribution |
| 10884521144132 | Primary | GS1 | 0 | |
| 30884521144136 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20884521144139 | 20884521144139 |
| 10884521144132 | 10884521144132 |
| 30884521144136 | 30884521144136 |
GMDN Terms#
| Term | Definition |
|---|---|
| ENFit oral/enteral syringe, single-use | A manual device intended to be used for the administration of oral medication or delivery of enteral nutrition by connection to an enteral administration device. It consists of a calibrated hollow barrel (cylinder) and a moveable plunger intended to be operated by a healthcare provider or parent device. The tip is designed to mate only with enteral administration devices (i.e., ENFit) and is incompatible with Luer connectors; the device may be colour-coded to distinguish it from syringes designed to mate with infusion/injection devices. It may include appropriate accessories (e.g., cap, bottle adaptor). This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Total Volume | 10 | Milliliter |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry;AVOID DIRECT SUNLIGHT |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 080935429
- Device count
- 100
- 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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10884521015791 | Dover | 8887623125 | 8887623125 | 2016-09-24 |
| 10884521153219 | Monoject | 1186060265 | 1186060265 | 2016-09-24 |
| 10884527021932 | Uni-Patch | EP84580 | EP84580 | 2016-09-24 |
| 20884521012216 | Monoject | 8881535788 | 8881535788 | 2016-09-24 |
| 20884521012254 | Monoject | 8881560182 | 8881560182 | 2016-09-24 |
| 20884521014159 | Monoject | 8881516135 | 8881516135 | 2016-10-13 |
| 10884521015920 | Dover | 20512C | 20512C | 2016-09-24 |
| 10884521015982 | Dover | 20520C | 20520C | 2016-09-24 |
| 10884521016002 | Dover | 20522C | 20522C | 2016-10-13 |
| 10884521024991 | Kendall | 9240 | 9240 | 2018-06-27 |
| 10884521025004 | Kendall | 9242 | 9242 | 2018-06-27 |
| 10884521025011 | Kendall | 9243 | 9243 | 2018-06-27 |
| 10884521025028 | Kendall | 9244 | 9244 | 2018-06-27 |
| 20192253002062 | Curity | 2146 | 2146- | 2018-12-12 |
| 20884521143064 | Magellan | 8881833515 | 8881833515 | 2016-09-24 |
| 10884527007110 | Argyle | 8888163055 | 8888163055 | 2016-09-24 |
| 10885380173691 | Curity | 6309G | 6309G | 2019-11-14 |
| 20885380173544 | Curity | 9022G | 9022G | 2019-11-14 |
| 20885380173568 | Curity | 9024G | 9024G | 2019-11-14 |
| 10884521141148 | Filac | 504083 | 504083 | 2016-09-24 |
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