FDA UDI
In Commercial Distribution
🇺🇸 United States
VASSALLO GT Hybrid
DI: 04582105830103
·
Model: VGT14300HYB
·
FILMEC K.K.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- VASSALLO GT Hybrid
- Primary DI
- 04582105830103
- Version / Model
- VGT14300HYB
- Catalog Number
- VGT14300HYB
- Company Name
- FILMEC K.K.
- Labeler DUNS
- 718142096
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-01-06
- Public Version
- 1
- Public Version Date
- 2023-01-16
- Public Version Status
- New
- Public Device Record Key
- d03b4d35-e566-4105-be95-4896865a6a1b
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DQX | Wire, Guide, Catheter | Cardiovascular | 870.1330 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 58115 | Peripheral vascular guidewire, manual | A long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 14582105830100 | GS1 | 5 | In Commercial Distribution | ||
| Primary | 04582105830103 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K203529 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 300 | Centimeter | |
| Outer Diameter | 0.014 | Inch |