Cragg Mc-Namara Valved Infusion Catheter
- Primary DI
- 00763000272425
- Brand
- Cragg Mc-Namara Valved Infusion Catheter
- Company
- Micro Therapeutics, Inc.
- Model
- 41050-01
- Device description
- INF CATH 41050-01 CRAGG-MC V07 ATHLONE
- Published
- 2020-11-13
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | General Hospital | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K940634 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00763000272425 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00763000272425 | 00763000272425 | 763000272425 | 0763000272425 |
GMDN Terms#
| Term | Definition |
|---|---|
| Peripheral vascular intervention infusion catheter | A flexible tube designed primarily to enable the delivery of diagnostic or therapeutic solutions into the peripheral vasculature during a cardiovascular procedure (e.g., delivery of an antithrombotic agent); some types may in addition be applied to coronary or pulmonary vasculature. It is percutaneously introduced and may include features such as side holes for infusion across a specific region, an expanding frame to disrupt clotted blood to improve diffusion, or a balloon to support infusion at a specific region. It is neither a peripherally-inserted central venous catheter, dedicated occluding catheter, nor superselective small vessel microcatheter. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | This device should be stored in a dry place, away from sunlight. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 826110710
- Device count
- 1
- Lot or batch
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00763000974077 | Riptide™ | MAT-110-110 | 2026-03-30 | |
| 00763000290702 | Instant Detacher | ID-1-5 | 2023-01-30 | |
| 00763000950750 | Riptide™ Aspiration Pump | MAP-1000 | 2026-03-09 | |
| 00763000491772 | Avyon™ 8FR Balloon Guide Catheter | 8F-087-85CM | 2021-04-15 | |
| 00763000491789 | Avyon™ 8FR Balloon Guide Catheter | 8F-087-95CM | 2021-04-15 | |
| 00763000915681 | Riptide™ Aspiration Pump | LMT-RAP | 2025-08-18 | |
| 00763000925338 | OnyxTM Liquid Embolic System (LES) | 105-7100-060 | 2026-01-02 | |
| 00763000925352 | OnyxTM Liquid Embolic System (LES) | 105-7100-080 | 2026-01-02 | |
| 00847536026834 | RebarTM | 105-5081-153 | 2017-04-14 | |
| 00763000974091 | Riptide™ | MAC-1200 | 2025-12-13 | |
| 00763000294236 | HyperForm | 104-4420 | 2020-08-01 | |
| 00763000294298 | HyperForm | 104-4715 | 2020-08-01 | |
| 00836462002180 | RebarTM | 105-5081-130 | 2015-10-09 | |
| 00847536005471 | HyperFormTM | 104-4420 | 2016-08-19 | |
| 00847536005549 | HyperFormTM | 104-4470 | 2016-04-05 | |
| 00847536005792 | HyperFormTM | 104-4715 | 2016-08-14 | |
| 00836462002197 | Rebar | 105-5081-153 | 2015-10-22 | |
| 00763000294267 | HyperForm | 104-4470 | 2020-08-01 | |
| 00763000294328 | HyperForm | 104-4770 | 2020-08-01 | |
| 00836462002135 | Rebar | 105-5080-153 | 2015-10-09 |
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|---|---|---|---|---|
| 08032248007123 | SOL CARE T | DELTA MED SPA | FOZ | 2021-03-30 |
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