Identity
- Trade Name
- Concentric 7F FDA UDI
- Generic Name
- Intravascular occluding balloon catheter, image-guided FDA UDI
- Device Name
- Balloon Guide Catheter FDA UDI
- Model / Reference
- 90072 FDA UDI
- Description
- Balloon Guide Catheter FDA UDI
Identifiers
- Catalog Number
- 90072 FDA UDI
- Primary DI / UDI-DI
- 00815742000726 FDA UDI
- 510(k) Number
- K112404 FDA UDI
- FDA Product Code
- DQY FDA UDI
- GMDN Term
- Intravascular occluding balloon catheter, image-guided FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 95.0 Centimeter FDA UDICatheter Gauge — 7.0 French FDA UDI
Category: Intravascular occluding balloon catheter, image-guided
Concentric 7F by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular occluding balloon catheter, image-guided.
- HyperGlide — Micro Therapeutics, Inc. · Class II
- Q50 Plus — QXMedical, LLC · Class II
- Polyurethane Dual Lumen Occlusion Catheter — LeMaitre Vascular, Inc. · Class II
- BOBBY/SOFIA Kit — MICROVENTION INC. · Class II
- Pennig Minifixator — Orthofix, Inc. · Class II
- LMI BILUMEN IRRIGATION ARTERIAL EMBOLECTOMY CATHETER — LUCAS MEDICAL INC · Class II
- HyperFormTM — Micro Therapeutics, Inc. · Class II
- CELLO™, Balloon Guide Catheter — Fuji Systems Corp. · Class II
Cleared under the same submission
K112404 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 3fcc7d4f-8a4e-4a24-952a-5b5f1275a0bd 38 fields · synced May 31, 2026