FDA UDI
Not in Commercial Distribution
🇺🇸 United States
Peregrine System™ Infusion Catheter
DI: 00862468000356
·
Model: FG32112
·
ABLATIVE SOLUTIONS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Peregrine System™ Infusion Catheter
- Primary DI
- 00862468000356
- Version / Model
- FG32112
- Company Name
- ABLATIVE SOLUTIONS, INC.
- Labeler DUNS
- 078293273
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2024-02-27
- Public Version
- 2
- Public Version Date
- 2025-11-04
- Public Version Status
- Update
- Public Device Record Key
- 7b2ea29b-209f-441a-ad50-d62cb5b5fd76
- Distribution End Date
- 2024-02-28
Device Description
Peregrine System™ Infusion Catheter (3-4 mm), 510k, US
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
- Yes
- 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
- Yes
- 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 |
|---|---|---|---|---|
| KRA | Catheter, Continuous Flush | Cardiovascular | 870.1210 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 32151 | Peripheral vascular intervention infusion catheter | A flexible tube designed primarily to enable the delivery of diagnostic or therapeutic solutions into the peripheral vasculature during a cardiovascular procedure (e.g., delivery of an antithrombotic agent); some types may in addition be applied to coronary or pulmonary vasculature. It is percutaneously introduced and may include features such as side holes for infusion across a specific region, an expanding frame to disrupt clotted blood to improve diffusion, or a balloon to support infusion at a specific region. It is neither a peripherally-inserted central venous catheter, dedicated occluding catheter, nor superselective small vessel microcatheter. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00862468000356 | GS1 |
Customer Contacts
- Phone
- 650 688-9743
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K231279 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 86 | Centimeter | |
| Device Size Text, specify | 3-4mm | ||
| Outer Diameter | 0.077 | Inch |