ENVOY
- Primary DI
- 10886704075073
- Brand
- ENVOY
- Company
- Medos International Sàrl
- Model
- 671-256-95D
- Catalog number
- 67125695D
- Device description
- ENVOY DA Guiding Catheter MPC 95cm 6F (2.0mm) 0.071 Inches (1.8mm)
- Published
- 2016-06-30
- 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
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 |
|---|---|
| K140080 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10886704075073 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10886704075073 | 10886704075073 |
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. |
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 482661753
- 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
- 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#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705034369761 | SKYLINE | 410270112 | 410270112 | 2016-12-31 |
| 10705034369778 | SKYLINE | 410270116 | 410270116 | 2016-12-31 |
| 10705034369785 | SKYLINE | 410270120 | 410270120 | 2016-12-31 |
| 10705034369822 | SKYLINE | 410270228 | 410270228 | 2016-12-31 |
| 10705034369839 | SKYLINE | 410270232 | 410270232 | 2016-12-31 |
| 10705034369846 | SKYLINE | 410270236 | 410270236 | 2016-12-31 |
| 10705034369884 | SKYLINE | 410270342 | 410270342 | 2016-12-31 |
| 10705034369891 | SKYLINE | 410270348 | 410270348 | 2016-12-31 |
| 10705034369907 | SKYLINE | 410270354 | 410270354 | 2016-12-31 |
| 10705034369983 | SKYLINE | 410290130 | 410290130 | 2016-12-31 |
| 10705034648194 | VELYS | 451611065 | 451611065 | 2026-10-09 |
| 10705034648200 | VELYS | 451611064 | 451611064 | 2026-10-09 |
| 00856879006519 | FIBERGRAFT Aeridyan | 59000170 | 59000170 | 2026-09-29 |
| 00856879006908 | FIBERGRAFT Aeridyan Matrix | 73000030 | 73000030 | 2023-04-05 |
| 00856879006915 | FIBERGRAFT Aeridyan Matrix | 73000063 | 73000063 | 2023-04-05 |
| 00856879006922 | FIBERGRAFT Aeridyan Matrix | 73000125 | 73000125 | 2023-04-05 |
| 00856879006946 | FIBERGRAFT Aeridyan Matrix | 73000200 | 73000200 | 2023-04-05 |
| 00856879006250 | FIBERGRAFT Aeridyan Matrix | 59000125 | 59000125 | 2021-08-04 |
| 00856879006281 | FIBERGRAFT Aeridyan Matrix | 59000063 | 59000063 | 2021-08-04 |
| 00856879006298 | FIBERGRAFT Aeridyan Matrix | 59000015 | 59000015 | 2021-08-04 |
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