Argyle
- Primary DI
- 00884521029319
- Brand
- Argyle
- Company
- Cardinal Health, Inc.
- Model
- 8888561076
- Catalog number
- 8888561076
- Device description
- Trocar Catheter,Sharp Tip
- Published
- 2017-05-09
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| DRC | Trocar |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| DRC | Trocar | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00884521029319 | Package | GS1 | 10 | In Commercial Distribution |
| 10884521029316 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00884521029319 | 00884521029319 | 884521029319 | 0884521029319 |
| 10884521029316 | 10884521029316 |
GMDN Terms
| Term | Definition |
|---|---|
| Closed-wound drain, non-bioabsorbable | A tube-like, non-bioabsorbable device designed to establish a channel for the removal of fluid or purulent material from a closed-wound or an infected area, typically used with a closed drainage system that applies a low negative pressure through the drain lumen. It is typically made of silicone and comes in various designs/sizes for a variety of surgical applications (e.g., orthopaedic, plastic/reconstructive, neurological, gynaecological, thoracic, cardiovascular, general surgery). It might include disposable devices dedicated to drain insertion/function (e.g., sharp trocar blade, connector), however it does not include any fluid collection bags/containers. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 32 | French |
| Length | 15.75 | Inch |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry;AVOID DIRECT SUNLIGHT |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(508)261-8000 | covidien.udi@covidien.com |
Regulatory Flags
- DUNS number
- 080935429
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- true
- 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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|---|---|---|---|---|
| 20884521014937 | Monoject | 8881511110 | 8881511110 | 2016-09-24 |
| 20884521014944 | Monoject | 8881511136 | 8881511136 | 2016-09-24 |
| 20884521025674 | Dover | 8884732598 | 8884732598 | 2016-09-24 |
| 20884527021434 | Kendall | 33503 | 33503 | 2016-09-24 |
| 20884527021441 | Kendall | 33504 | 33504 | 2016-09-24 |
| 20884527021458 | Kendall | 33505 | 33505 | 2016-09-24 |
| 20884527021465 | Kendall | 33506 | 33506 | 2016-09-24 |
| 20884527021472 | Kendall | 33507 | 33507 | 2016-09-24 |
| 20884527021489 | Kendall | 33508 | 33508 | 2016-09-24 |
| 20884527021502 | Kendall | 33510 | 33510 | 2016-09-24 |
| 30884521012442 | Monoject | 8881202314 | 8881202314 | 2018-06-27 |
| 20884521012469 | Monoject | 8881202322 | 8881202322 | 2018-06-27 |
| 30884521012473 | Monoject | 8881202330 | 8881202330 | 2018-06-27 |
| 30884521012497 | Monoject | 8881202348 | 8881202348 | 2018-06-27 |
| 30884521012534 | Monoject | 8881202371 | 8881202371 | 2018-06-30 |
| 30884521012558 | Monoject | 8881202389 | 8881202389 | 2018-06-27 |
| 20884521012568 | Monoject | 8881202397 | 8881202397 | 2018-06-30 |
| 20884521142760 | Monoject | 10884521142763 | 10884521142763 | 2018-06-29 |
| 00029369211032 | MCDAVID | MH79400 | 211 | 2023-05-26 |
| 90884521162088 | Uni-Patch | MH73912 | MH73912 | 2018-06-30 |
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| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
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