Launcher
- Primary DI
- 10721902590549
- Brand
- Launcher
- Company
- MEDTRONIC, INC.
- Model
- LA7CHAMP25
- Device description
- CATHETER LA7CHAMP25 LA 7F 100CM CH25
- Published
- 2016-05-27
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DQY | CATHETER, PERCUTANEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DQY | Catheter, Percutaneous | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K022764 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10721902590549 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10721902590549 | 10721902590549 |
GMDN Terms#
| Term | Definition |
|---|---|
| Vascular guide-catheter, single-use | A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes. It is not intended solely for infusion nor to access superselective small vessels, and does not include a transseptal needle. A percutaneous introduction set, shaft visualization electrodes, or haemostatic valve may be supplied with the guide-catheter. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 0 | |
| Device Size Text, specify | 0 | |
| Length | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Store catheters straight in a cool dark area. Do not expose catheters to solvents or ionizing radiation. |
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 006261481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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 |
|---|---|---|---|---|
| 00643169013995 | NA | 207211A | 2017-02-02 | |
| 00643169014008 | NA | 207211 | 2017-02-02 | |
| 00643169014039 | NA | 206211A | 2017-02-02 | |
| 00643169014046 | NA | 206211 | 2017-02-02 | |
| 00643169014053 | NA | 205211A | 2017-02-02 | |
| 00643169014060 | NA | 205211 | 2017-02-02 | |
| 00643169014077 | INPUT™ TS | 091102A | 2017-02-02 | |
| 00643169014084 | INPUT™ TS | 091101A | 2017-02-03 | |
| 00643169014091 | INPUT™ TS | 090037A | 2017-02-02 | |
| 00643169014107 | INPUT™ PS | 090023 | 2017-02-02 | |
| 00643169014121 | INPUT™ PS | 893311 | 2017-02-02 | |
| 00643169014138 | INPUT™ PS | 883311 | 2017-02-03 | |
| 00643169014145 | INPUT™ PS | 873311 | 2017-02-03 | |
| 00643169014152 | INPUT™ PS | 863311 | 2017-02-02 | |
| 00643169014169 | INPUT™ PS | 853311 | 2017-02-02 | |
| 00643169014176 | NA | 693311 | 2016-08-20 | |
| 00643169014213 | NA | 663311 | 2017-02-02 | |
| 00643169014220 | NA | 653311 | 2017-02-02 | |
| 00643169014237 | INPUT™ PS | 593311 | 2017-02-03 | |
| 00643169014244 | INPUT™ PS | 583311 | 2017-02-02 |
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| 00857545008158 | Zebra | Q'APEL MEDICAL LLC | DQY | 2025-01-03 |
| 00857545008165 | Zebra | Q'APEL MEDICAL LLC | DQY | 2025-01-03 |
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