FDA UDI
In Commercial Distribution
🇺🇸 United States
Bridge Plus occlusion balloon
DI: 00810060550816
·
Model: 590-002
·
Philips Image Guided Therapy Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
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Basic Information
- Brand Name
- Bridge Plus occlusion balloon
- Primary DI
- 00810060550816
- Version / Model
- 590-002
- Catalog Number
- 590-002
- Company Name
- Philips Image Guided Therapy Corporation
- Labeler DUNS
- 118354223
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-10-09
- Public Version
- 1
- Public Version Date
- 2025-10-17
- Public Version Status
- New
- Public Device Record Key
- 05e6a432-0e2c-4185-bb01-4bc365220c74
Device Description
Bridge Plus Occlusion Balloon Catheter
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
- 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 |
|---|---|---|---|---|
| MJN | Catheter, Intravascular Occluding, Temporary | Cardiovascular | 870.4450 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 32584 | Intravascular occluding balloon catheter, image-guided | A non-powered flexible tube with an inflatable balloon(s) at the distal end intended to be introduced short-term under image guidance to temporarily block a blood vessel. It may be used for arteriography, selective angiography, preoperative occlusion, peripheral and intracranial vasculature occlusion, emergency control of haemorrhage, to treat aneurysms, chemotherapeutic drug infusion, and renal opacification procedures. It may have a dual- or multi-lumen design for balloon inflation, introduction over a guidewire, infusion of contrast medium, or delivery of a smaller catheter or embolic agents; some types have graduated markings to assist insertion. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00810060550816 | GS1 |
Customer Contacts
- Phone
- (800) 228-4728
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K251358 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Introducer Sheath Compatibility | 12 | French | |
| Balloon Diameter | 29 | Millimeter | |
| Balloon Length | 80 | Millimeter | |
| Catheter Working Length | 90 | Centimeter | |
| Device Size Text, specify | Guidewire Compatibility: 0.035 Inch |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Keep dry
- Type
- Special Storage Condition, Specify
- Special Conditions
- Keep away from sunlight