ENVI
- Primary DI
- H965355070
- Brand
- ENVI
- Company
- NAVILYST MEDICAL, INC.
- Model
- 35-507
- Device description
- NVI MINI STICK 6F X 20 CM .018 Ni/Tu 21G TROCAR
- Published
- 2017-08-07
- 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
Product Codes
| Code | Name |
|---|---|
| DYB | INTRODUCER, CATHETER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| DYB | Introducer, Catheter | Cardiovascular | 2 |
Premarket Submissions
| Submission | Supplement |
|---|---|
| K170775 | 000 |
Premarket Details
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| H965355071 | Package | HIBCC | 5 | In Commercial Distribution |
| H965355070 | Primary | HIBCC | 0 | |
| 15051684023603 | Secondary | GS1 | 0 |
GMDN Terms
| Term | Definition |
|---|---|
| Vascular catheter introduction set, nonimplantable | A collection of sterile, nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 6 | French |
| Length | 20 | Centimeter |
| Lumen/Inner Diameter | 0.5 | Millimeter |
| Needle Gauge | 21 | Gauge |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(518)795-1676 | dgreer@angiodynamics.com |
Regulatory Flags
- DUNS number
- 809699023
- 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 |
|---|---|---|---|---|
| H787CT50LPBANFVI0 | BioFlo Vortex | CT50LPBANFVI | 2020-05-29 | |
| H787CT50LPBAVI0 | BioFlo Vortex | CT50LPBAVI | 2020-05-29 | |
| H787CT50LPBDNFVI0 | BioFlo Vortex | CT50LPBDNFVI | 2020-05-29 | |
| H787CT50LPBDVI0 | BioFlo Vortex | CT50LPBDVI | 2020-05-29 | |
| H787CT50LTBANFVI0 | BioFlo Vortex | CT50LTBANFVI | 2020-05-29 | |
| H787CT50LTBAVI0 | BioFlo Vortex | CT50LTBAVI | 2020-05-29 | |
| H787CT50LTBDNFVI0 | BioFlo Vortex | CT50LTBDNFVI | 2020-05-29 | |
| H787CT50LTBDVI0 | BioFlo Vortex | CT50LTBDVI | 2020-05-29 | |
| H787CT50PTBANFVI0 | BioFlo Vortex | CT50PTBANFVI | 2020-05-29 | |
| H787CT50PTBAVI0 | BioFlo Vortex | CT50PTBAVI | 2020-05-29 | |
| H787CT50PTBDNFVI0 | BioFlo Vortex | CT50PTBDNFVI | 2020-05-29 | |
| H787CT50PTBDVI0 | BioFlo Vortex | CT50PTBDVI | 2020-05-29 | |
| H787CT50STBDNFVI0 | BioFlo Vortex | CT50STBDNFVI | 2020-05-29 | |
| H787CT50STBDVI0 | BioFlo Vortex | CT50STBDVI | 2020-05-29 | |
| H787CT60LPBANFVI0 | BioFlo Vortex | CT60LPBANFVI | 2020-05-29 | |
| H787CT60LPBAVI0 | BioFlo Vortex | CT60LPBAVI | 2020-05-29 | |
| H787CT60LPBDNFVI0 | BioFlo Vortex | CT60LPBDNFVI | 2020-05-29 | |
| H787CT60LPBDVI0 | BioFlo Vortex | CT60LPBDVI | 2020-05-29 | |
| H787CT60LPPANFNV0 | BioFlo Vortex | CT60LPPANFNV | 2020-05-29 | |
| H787CT60LPPANFVI0 | BioFlo Vortex | CT60LPPANFVI | 2020-05-29 |
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