AMPHIRION DEEP
- Primary DI
- 08033477045733
- Brand
- AMPHIRION DEEP
- Company
- MEDTRONIC, INC.
- Model
- AMP354210002
- Device description
- CATH AMP354210002 AMP US 03.5-4L210 UL12
- Published
- 2016-05-07
- Public version status
- Update
- Distribution status
- Not 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 |
|---|---|
| DQY | CATHETER, PERCUTANEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DQY | Catheter, Percutaneous | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K083919 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08033477045733 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08033477045733 | 08033477045733 | 8033477045733 |
GMDN Terms#
| Term | Definition |
|---|---|
| Peripheral angioplasty balloon catheter, basic | A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Length | 210 | Millimeter |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Store at controlled room temperature in dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 006261481
- Device count
- 1
- Lot or batch
- true
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| 00763000422615 | SYNCHROMED®II | 8637-40 | 2021-04-11 | |
| 00763000634094 | SYNCHROMED® II | 8637-20 | 2022-08-11 | |
| 00763000634100 | SYNCHROMED® II | 8637-40 | 2022-08-11 | |
| 00643169508149 | SYNCHROMED® II | 8637-20 | 2016-04-27 | |
| 00643169508156 | SYNCHROMED® II | 8637-40 | 2016-04-27 | |
| 00643169630505 | SYNCHROMED® II | 8637-20 | 2018-08-17 | |
| 00643169630512 | SYNCHROMED® II | 8637-40 | 2018-08-17 | |
| 00643169100824 | SYNCHROMED ® II | 8637-40 | 2016-04-27 | |
| 00643169100831 | SYNCHROMED ® II | 8637-20 | 2016-04-27 | |
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